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.

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.

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.

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

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.

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.

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.

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.

Durable and recyclable BiOBr/silk fibroin-cellulose acetate composite film for efficient photodegradation of dyes under visible light irradiation

A stable and recyclable of BiOBr/silk fibroincellulose acetate composite film was prepared by blendingwet phase transformation and in situ precipitate technology.The cellulose acetate film modified by silk fibroin formed a finger-shaped porous structure,which provided a large space for the uniform growth of BiOBr nanosheets and facilitated the shuttle flow of dyes in film.The morphology,phase structure,and optical properties of the composite films were characterized using various techniques,and their photocatalytic performance for dye wastewater was evaluated under visible light irradiation.Results showed that the BiOBr/SF-CA composite film exhibited efficient photocatalytic activity with 99.9%of rhodamine B degradation rate.Moreover,the composite film maintained high catalytic stability because Bi as the active species deposited on the film showed almost no loss.Finally,the possible photocatalytic mechanisms in the BiOBr/SF-CA composite film were speculated through radical-trapping experiments and electron spin resonance testing.

Facile Synthesis of Cellulose Acetate Ultrafiltration Membrane with Stimuli-Responsiveness to pH and Temperature Using the Additive of F127-b-PDMAEMA

We fabricate a novel cellulose acetate （CA） ultrafiltration membrane modified by block copolymer F127-b- PDMAEMA, which is synthesized using F127 and DMAEMA via the ARGET ATRP method. Compared to conven- tional ultrafiltration membranes, the incorporation of both F 127 and PDMAEMA can not only readily increase the hydrophilicity of the membrane, but also exhibit stimuli-responsiveness to temperature and pH. Fourier transform infrared spectroscopy （FT-IR）, nuclear magnetic resonance spectroscopy （NMR）, and gel permeation chromatog- raphy （GPC） are employed to analyze the structure of the F 127-b-PDMAEMA. The membrane properties are eval- uated via scanning electron microscope （SEM） imaging, porosity test, automatic target recognition Fourier trans- form infrared spectroscopy （ATR-FTIR）, water contact angle test and permeation test. The results indicate that the F 127-b-PDMAEMA is an excellent pore agent, which contributes to an enhancement of the membrane in sensitivity to temperature and pH. The modified membrane also exhibits lower water contact angle （64.5~）, which is attributed to the good anti-fouling performance and high water permeation.

PREPARATION AND CHARACTERIZATION OF ELECTROSPUN FIBERS BASED ON POLY(L-LACTIC ACID)/CELLULOSE ACETATE

PLLA/CA mixtures of different compositions were successfully electrospun to obtain composite nanofibrous membranes. The microstructures of the membrances changed from homogeneous to heterogeneous with the addition of CA, which was observed by FE-ESEM. The PLLA/CA fabric membranes were characterized by mechanical testing, DSC and contact angle measurements. The tensile stress of the composite fibrous membranes increased obviously with the increase of CA content. DSC results indicated that the CA component was the main factor for the changes of enthalpies in the composite fibers. Contact angle measurements showed the hydrophilicity of the electrospun nanofiber membranes was improved with the addition of CA.

Piezoelectric Nanogenerator Based on Electrospun Cellulose Acetate/Nanocellulose Crystal Composite Membranes for Energy Harvesting Application

Nanogenerators,as the typical conversion of mechanical energy to electrical energy devices,have great potential in the application of providing sustainable energy sources for powering miniature devices.In this work,cellulose acetate/cellulose nanocrystal(CA/CNC)composite nanofiber membranes were prepared by electrospinning method and then utilized to manufacture a flexible pressure-driven nanogenerator.The addition of CNC not only increased the content of piezoelectric cellulose I crystallization but also strengthened the mechanical deformation of the nanofiber membranes,which could greatly enhance the piezoelectric performance of CA/CNC composite membranes.The CA/CNC composite nanofiber membrane with 20%(mass fraction)of CNC(CA/CNC-20%)showed optimal piezoelectric conversion performance with the output voltage of 1.2 V under the force of 5 N(frequency of 2 Hz).Furthermore,the output voltage of the CA/CNC-20%nanogenerator device exhibited a linear relationship with applied impact force,indicating the great potential in pressure sensors.

Fabrication and performance of PET mesh enhanced cellulose acetate membranes for forward osmosis

Polyethylene terephthalate mesh（PET） enhanced cellulose acetate membranes were fabricated via a phase inversion process. The membrane fabrication parameters that may affect the membrane performance were systematically evaluated including the concentration and temperature of the casting polymer solution and the temperature and time of the evaporation, coagulation and annealing processes. The water permeability and reverse salt flux were measured in forward osmosis（FO） mode for determination of the optimal membrane fabrication conditions. The optimal FO membrane shows a typical asymmetric sandwich structure with a mean thickness of about 148.2 μm. The performance of the optimal FO membrane was tested using 0.2 mol/L Na Cl as the feed solution and 1.5 mol/L glucose as the draw solution. The membrane displayed a water flux of 3.47 L/（m2·hr） and salt rejection of95.48% in FO mode. While in pressure retarded osmosis（PRO） mode, the water flux was4.74 L/（m2·hr） and salt rejection 96.03%. The high ratio of water flux in FO mode to that in PRO mode indicates that the fabricated membrane has a lower degree of internal concentration polarization than comparable membranes.

Tailoring nanocomposite membranes of cellulose acetate/silica nanoparticles for desalination

Herein, the fabrication of cellulose acetate (CA) silica-based nanocomposite membranes via the dry-wetphase inversion procedure for water desalination was investigated. The modified and unmodified silicananoparticles (MSNPs and SNPs) were prepared by the sol-gel technique. The effect of the SNPs andMSNPs was investigated on the CA membrane's properties and their performance for water desalination.The CA nanocomposite membranes were characterized to study their structure, hydrophilicity, andmorphology. The fabricated nanocomposite membranes showed hydrophilic surface properties. Theperformance of reverse osmosis (RO) membranes was measured using a crossflow RO unit at 10 bar(1 bar = 0.1 MPa). The membrane with 10 mg of SNPs enhanced permeate water flux compared to thepristine CA membrane by 1.6 L/(m2·h). The effect of MSNPs on the nanocomposites' performance waslower than their counterpart in the case of adding SNPs. The membrane with 30 mg of MSNPs showedthe highest permeate water flux among other nanocomposite membranes with a value oAQSf 35.7 L/(m2·h)at 24 bar.