Cellulose Paper Research Articles

Plasticizer-based and polymer-free ion-selective optodes on cellulose paper

Paper-based ion-selective optodes (ISOs) allow for low-cost ion measurements using widely accessible optical detectors such as smartphones, representing an attractive analytical platform for medical testing and environmental monitoring. Previously reported paper-based ISOs rely on plasticized PVC membranes or PVC/plasticizer-free adsorption layers containing hydrophobic sensing chemicals. In this paper, we studied a new format of paper-based ISOs, in which a plasticizer phase containing sensing chemicals is deposited onto cellulose paper without using a hydrophobic polymer like PVC. Compared to ISOs without plasticizers and polymers, the plasticizer-based ISOs show much higher pH sensitivity when using chromoionophore I and tetrakis[3,5-bis(trifluoromethyl)phenyl]borate as the sensing chemicals. When the sensing layer further contains a solid ionophore with high molecular rigidity, the plasticizer-based ISOs for cations also exhibit enhanced sensitivity than the plasticizer-free ISOs. However, when the ionophore is a liquid at room temperature or has a long alkyl chain, the plasticizer-based and plasticizer-free ISOs have comparable responses because the ionophore behaves as a pseudo-plasticizer. Compared to ISOs with both plasticizers and polymers, the elimination of hydrophobic polymers like PVC makes inkjet printing more efficient and preserves the capillary action of the porous paper. By using the newly launched Samba cartridge with smaller nozzles, the plasticizer-based and polymer-free optodes for sodium, potassium, and calcium ions are prepared by inkjet printing for the first time. In an example application, the inkjet-printed plasticizer-based and polymer-free ISOs are used for colorimetric measurements of urine calcium.

Flexible photodetector for broadband detection using wurtzite phase CuFeS2 nanoparticles

In the realm of electronic devices, a rising demand for flexible and enhanced performance has emerged. Current research predominately centres on optoelectronics and sensors within the flexible devices’ domain. A flexible photodetector, utilizing CuFeS2 (CFS), is crafted on a cellulose paper substrate. Employing the hand printing method, a thin film of CFS on a graphene-based transporting layer is fabricated. The wurtzite phase of the material synthesized using microwave−assisted method is confirmed by X−ray diffraction (XRD) and Raman spectroscopy, with compositional details provided by energy dispersive X−ray analysis. Comprehensive XRD based calculations of size, stress, strain and energy density are conducted using three different models - Uniform Deformation Model, Uniform Stress Deformation Model and Uniform Deformation Energy Density Model. The average particle size, strain and stress from the three different models is found to be 9⋅73 nm, 1⋅35 × 10−3, 55⋅05 MPa along with calculated energy density value of 78⋅421 kJ m−3, respectively. Band gap calculations utilizing diffuse reflectance yielded an optical bandgap of 1⋅23 eV for the CFS thin film. The fabricated photodetector is studied for different illumination wavelengths, 450 nm, 520 nm, 570 nm, 620 nm and 940 nm, to determined device parameters. The optimum rise time, decay time, responsivity, and specific detectivity for wavelength of 520 nm are 6⋅43 s, 7⋅01 s, 0⋅0319 mA W−1 and 1⋅173 × 1010 Jones. The photoresponse of the fabricated device bended to 2⋅5− and 5−mm radii is studied to recognize suppleness. The photoresponse showed the photocurrent decreases with increase of bending. The observed traits under bending switched to initial on flattening the thin film.

Evaluation of Chitosan Activity Produced Via Biotransformation of Chitin Against Some Pathogens Associated with Burn Infection in Vitro and in Vivo

Burn infections are a serious concern for patients with burn injuries, as they can lead to significant morbidity and mortality. The present study was designed to evaluate the chitosan activity against five pathogens collected from burn infections (Escherichia coli ZE15, Acinetobacter bummani ZA2, Klebsiella pneumonia ZK3 and Pseudomonas aeruginosa ZP17, Staphylococcus aureus ZS2). Chitosan was produced in solid-state fermentation using corn meal supplemented with 2% of shrimp shell chitin. The degree of deacetylation of chitosan was 79.5% and the FT-IR spectrum (4000 to 400) cm-1 gave IR spectra similar to that of the commercial chitosan. The produced chitosan showed a significant inhibitory ability from the concentration of 10 mg/ml to 2 mg/ml. The M.I.C. and S.I.C were varied between the isolates; for P. aeruginosa ZP17 and Staph. aureus ZS2, the M.I.C and S.I.C were 1.6 mg/ml and of 1.4 mg/ml respectively, while for E. coli ZE15, Kl. pneumonia ZK3 and A. bumannii ZA2 were 1.4 mg/ml and 1.2 mg/ml. Furthermore, this study showed an the important role of the produced chitosan as an antibiofilm agent to reduce the biofilm formation for the tested isolates. However, the strongest antibiofilm activity was against E. coli Z.E15 with 55.2%. Moreover, four potential formulas containing chitosan with concentration of 1.6 mg/ml were tested. A formula containing polyvinyl alcohol, vaseline and chitosan to create a cream showed the best results in comparison with the four-formula used in this study. This formula was added to pads of thick cellulosic filter paper to treat a mouse model with full thickness cutaneous burn to assess the benefits of treating with a chitosan dressing. The healing process was examined and results showed a signs of remodeling stage by day four and a scar tissue formation by day nine.

Antimicrobial and hydrophobic cellulose paper prepared by covalently attaching cinnamaldehyde for strawberries preservation

The demand for paper-based packaging materials as an alternative to incumbent disposable petroleum-derived polymers for food packaging applications is ever-growing. However, typical paper-based formats are not suitable for use in unconventional applications due to inherent limitations (e.g., excessive hydrophilicity, lack antimicrobial ability), and accordingly, enabling new capabilities is necessity. Herein, a simple and environmentally friendly strategy was proposed to introduce antimicrobial and hydrophobic functions to cellulose paper through successive chemical grafting of 3-aminopropyltriethoxysilane (APS) and cinnamaldehyde (CA). The results revealed that cellulose paper not only showed long-term antibacterial effect on different bacteria, but also inhibited a wide range of fungi. Encouragingly, the modified paper, which is fluorine-free, displays a high contact angle of 119.7°. Thus, even in the wet state, the modified paper can still maintain good mechanical strength. Meanwhile, the multifunctional composite papers have excellent biocompatibility and biodegradability. Compared with ordinary cellulose paper, multifunctional composite paper can effectively prolong the shelf life of strawberries. Therefore, the multifunctional composite paper represents good application potential as a fruit packaging material.

A disposable immunosensor array using cellulose paper assembled chemiresistive biosensor for simultaneous monitoring of mycotoxins AFB1 and FB1

Due to the common contamination of multiple mycotoxins in food, which results in stronger toxicity, it is particularly important to simultaneously test for various mycotoxins for the protection of human health. In this study, a disposable immunosensor array with low-cost was designed and fabricated using cellulose paper, polydimethylsiloxane (PDMS), and semiconducting single-walled carbon nanotubes (s-SWCNTs), which was modified with specific antibodies for mycotoxins AFB1 and FB1 detection. The strategy for fabricating the immunosensor array with two individual channels involved a two-step protocol starting with the form of two kinds of carbon films by depositing single-wall carbon nanotubes (SWCNTs) and s-SWCNTs on the cellulose paper as the conductive wire and sensing element, followed by the assembly of chemiresistive biosensor with SWCNTs strip as the wire and s-SWCNTs as the sensing element. After immobilizing AFB1-bovine serum albumin (AFB1-BSA) and FB1-bovine serum albumin (FB1-BSA) separately on the different sensing regions, the formation of mycotoxin-BSA-antibody immunocomplexes transfers to electrochemical signal, which would change with the different concentrations of free mycotoxins. Under optimal conditions, the immunosensor array achieved a limit of detection (LOD) of 0.46 pg/mL for AFB1 and 0.34 pg/mL for FB1 within a wide dynamic range from 1 pg/mL to 20 ng/mL. Furthermore, the AFB1 and FB1 spiked in the ground corn and wheat extracts were detected with satisfactory recoveries, demonstrating the excellent practicality of this established method for simultaneous detection of mycotoxins.

Improving the Barrier and Mechanical Properties of Paper Used for Packing Applications with Renewable Hydrophobic Coatings Derived from Camelina Oil.

This study looked at using modified camelina oil to develop sustainable coatings that could replace those derived from petroleum-based materials for use in packaging and other industrial sectors. Solvent-free synthesis of maleic anhydride grafted camelina oil (MCO) was carried out at two different temperatures (200 and 230 °C) to obtain sustainable hydrophobic coating materials for paper substrates. Maleic anhydride grafting of camelina oil was confirmed with attenuated total reflectance-Fourier transform infrared and NMR spectroscopic techniques, and up to 16% grafting of maleic anhydride was achieved, as determined by the titration method. MCO, obtained at different reaction temperatures, was coated onto cellulosic paper and evaluated for its hydrophobicity, mechanical, oxygen, and water vapor barrier properties. Scanning electron microscopy indicated the homogeneous dispersion of coating material onto the paper substrate. MCO-coated papers (MCO-200C paper and MCO-230C paper) provided a water contact angle of above 90° which indicates that the modified oil was working as a hydrophobic coating. Water vapor permeability (WVP) testing of coated papers revealed a reduction in WVP of up to 94% in comparison to the uncoated paper. Moreover, an improved oxygen barrier property was also observed for paper coated with both types of MCO. Analysis of the mechanical properties showed a greater than 70% retention of tensile strength and up to a five-fold increase in elongation at break of coated versus uncoated papers. Overall, the results show that camelina oil, a renewable resource, can be modified to produce environmentally friendly hydrophobic coating materials with improved mechanical and water vapor barrier properties that can serve as a potential coating material in the packaging industry. The results of this research could find applications in the huge paper packaging industries, specially in food packaging.

Hydrophobic sisal cellulose paper-based TENG for collecting rain energy and raindrop-based sensor

Hydrophobic Sisal cellulose paper (SCP) was obtained by surface modification of SCP via physical adsorbing polymer and chemical grafting monomer, respectively. The influence of surface modification conditioning on the hydrophobicity, dielectric constant and dipole moment of the SCP was investigated. The results showed that the hydrophobicity and dielectric constant of the modified SCP increased with the concentration and amount of the modifiers. The output electrical performance of the TENGs assembled by the two types of hydrophobic SCP for rain energy collection was compared. The output electrical performance of the chemically modified hydrophobic SCP-TENG is higher than that of the physical modified. The maximum power density of the former reaches 8.2 mW/m2. Furthermore, based on the linear relationship between the output performance (output voltage intensity and output current intensity) of hydrophobic SCP-TENG and the droplet velocity, a raindrop-based sensor based on hydrophobic SCP-TENG was successfully constructed and estimated.

Polymer composite membranes as SERS substrate materials: Recyclable and highly stable

Surface-enhanced Raman spectroscopy (SERS), as an emerging molecular-level detection technology, has attracted considerable research attention, especially in the context of substrate materials exhibiting Raman enhancement effects. Membrane materials, owing to their commendable uniformity, stability, and ease of modification, hold a pivotal position in the landscape of SERS substrate materials. However, existing SERS substrates based on membrane materials have limited adaptability to a spectrum of extreme environments, including but not limited to high or low pH, elevated salinity, and corrosive solutions. Additionally, SERS substrate materials are synonymous with “waste” and “high investment” because of their inherent disposable nature. This study introduces a pioneering approach, presenting a polymer composite membrane founded on epoxy resin, cellulose paper, and nanometal particles as a novel SERS substrate material. Given the outstanding stability of epoxy resin, the substrate material exhibits normal functionality in environments ranging from −80 ℃ to 100 ℃, with pH levels spanning 1 to 13, and in highly acidic solutions (concentration ≤3 %) and highly alkaline solutions (concentration ≤0.1 M). Moreover, the cleanability inherent in the polymer composite membrane renders the substrate material recyclable. Experimental findings reveal that even after six repeated uses, the substrate material sustains a stable Raman signal enhancement effect. The integration of recyclability and heightened stability makes this SERS substrate material a promising candidate for real-time monitoring and batch testing in chemical production processes or other complex environments.

Modification of cellulose substrate by in situ synthesis of metal-organic framework-5 for thin film microextraction of some non-steroidal anti-inflammatory drugs and their measurement by high-performance liquid chromatography-ultraviolet detector

This work, reports the successful preparation a thin film by a simple and inexpensive process for quantification of a model analytes in the urine sample using HPLC-UV. To this end, cellulose paper was employed as a substrate for the in-situ synthesis of MOF-5, to increase the resistance of the prepared film. The prepared film can be reused 26 times with no reduction in its performance. The thin film prepared by MOF-5 modified cellulose substrate was utilized in thin film microextraction (TFME) method for the extraction and preconcentration of naproxen, aspirin, tolmetin, and celecoxib. Under optimal conditions, the linear dynamic range of the target analytes was 2–500 µg L−1 with correlation coefficients (R2) ranging from 0.9961 to 0.9990. Also, the limits of detection (LODs), the limits of quantification (LOQs) and relative standard deviation (RSD%) of the proposed method for selected analytes ranged between 0.57 and 0.77 µg L−1, 1.7 to 2.3 and 3.5 % to 6.2 %, respectively. Moreover, relative recoveries varied from of 94 % to 108 %, indicating the absence of matrices effect in the proposed method. Eventually, the TFME was successfully used for the extraction of selected analytes from urine samples.

Differentiating Plasmon-Enhanced Chemical Reactions on AgPd Hollow Nanoplates through Surface-Enhanced Raman Spectroscopy.

Plasmonic photocatalysis demonstrates great potential for efficiently harnessing light energy. However, the underlying mechanisms remain enigmatic due to the transient nature of the reaction processes. Typically, plasmonic photocatalysis relies on the excitation of surface plasmon resonance (SPR) in plasmonic materials, such as metal nanoparticles, leading to the generation of high-energy or "hot electrons", albeit accompanied by photothermal heating or Joule effect. The ability of hot electrons to participate in chemical reactions is one of the key mechanisms, underlying the enhanced photocatalytic activity observed in plasmonic photocatalysis. Interestingly, surface-enhanced Raman scattering (SERS) spectroscopy allows the analysis of chemical reactions driven by hot electrons, as both SERS and hot electrons stem from the decay of SPR and occur at the hot spots. Herein, we propose a highly efficient SERS substrate based on cellulose paper loaded with either Ag nanoplates (Ag NPs) or AgPd hollow nanoplates (AgPd HNPs) for the in situ monitoring of C-C homocoupling reactions. The data analysis allowed us to disentangle the impact of hot electrons and the Joule effect on plasmon-enhanced photocatalysis. Computational simulations revealed an increase in the rate of excitation of hot carriers from single/isolated AgPd HNPs to an in-plane with a vertical stacking assembly, suggesting its promise as a photocatalyst under broadband light. In addition, the results suggest that the incorporation of Pd into an alloy with plasmonic properties may enhance its catalytic performance under light irradiation due to the collection of plasmon-excitation-induced hot electrons. This work has demonstrated the performance-oriented synthesis of hybrid nanostructures, providing a unique route to uncover the mechanism of plasmon-enhanced photocatalysis.

Foldable paper-based photoelectrochemical biosensor based on etching reaction of CoOOH nanosheets-coated laser-induced PbS/CdS/graphene for sensitive detection of ampicillin

Timely and rapid detection of antibiotic residues in the environment is conducive to safeguarding human health and promoting an ecological virtuous cycle. A foldable paper-based photoelectrochemical (PEC) sensor was successfully developed for the detection of ampicillin (AMP) based on glutathione/zirconium dioxide hollow nanorods/aptamer (GSH@ZrO2 HS@apt) modified cellulose paper as a reactive zone with laser direct-writing lead sulfide/cadmium sulfide/graphene (PbS/CdS/LIG) as photoelectrode and cobalt hydroxide (CoOOH) as a photoresist material. Initially, AMP was introduced into the paper-based reaction zone as a biogate aptamer, which specifically recognized the target and then left the ZrO2 HS surface, releasing glutathione (GSH) encapsulated inside. Subsequently, the introduction of GSH into the reaction region and etching of CoOOH nanosheets to expose the PbS/CdS/LIG photosensitive material increased photocurrent. Under optimal conditions, the paper-based PEC biosensor showed a linear response to AMP in the range of 5.0 - 2 × 104 pM with a detection limit of 1.36 pM (S/N = 3). In addition, the constructed PEC sensing platform has excellent selectivity, high stability and favorable reproducibility, and can be used to assess AMP residue levels in various real water samples (milk, tap water, river water), indicating its promising application in environmental antibiotic detection.

Highly water-resistant paper via infiltration with polymeric microspheres from nanocellulose-stabilized plant oil-derived monomer

Sustainable strategies to improve the water resistance of cellulose paper are actively sought. In this work, polymeric microspheres (PMs), prepared through emulsion polymerization of cellulose nanofibers stabilized rubber seed oil-derived monomer, were investigated as coatings on corrugated medium paper (CMP). After infiltrating porous paper with PMs, the water-resistant corrugated papers (WRCPn) with enhanced mechanical properties were obtained. When 30 wt% PMs were introduced, WRCP30 turned out to be highly compacted with an increased water contact angle of 106.3° and a low water vapor transmission rate of 81 g/(m2 d) at 23 °C. Meanwhile, the tensile strength of WRCP30 increased to 22.2 MPa, a 4-fold increase from CMP. When tested in a well-hydrated state, 71% of its mechanical strength in the dry state was maintained. Even with a low content of 10 wt% PMs, WRCP10 also exhibited stable tensile strength and water wettability during the cyclic soaking-drying process. Thus, the plant oil based sustainable emulsion polymers provide a convenient route for enhancing the overall performance of cellulose paper.

Dimethyl Amine Detection using Polydiacetylene Functionalized Cellulose Paper

AbstractThis work demonstrates our effort to develop stimuli responsive cellulose films for the detection of dimethyl amines, a biogenic amine, released during food decomposition. Herein, we demonstrate that thin layer deposition of polydiacetylene‐zinc oxide nanosheets (PDA‐ZnO) on cellulose (CE) paper yields a stimuli responsive strip exhibiting strong thermochromism and solvatochromism against dimethyl amine. The incorporation of Zn nanoclusters within the composite plays an essential role in achieving reversible thermochromism while strong intermolecular interactions promote adsorption of PDA‐ZnO on cellulose paper. X‐ray diffraction and infrared spectroscopy reveal that the Zn2+ ions intercalate with PDA bilayer and strongly interact with the carboxylate headgroup of PDA. Furthermore, the reversible thermochromism persist when the nanosheets are deposited on cellulose (CE) paper when assembling PDA‐ZnO−CE paper. In addition, PDA‐ZnO−CE displayed selective solvatochromism allowing the utilization of the paper in the detection of dimethyl amine as it displayed a distinct and remarkable purple to orange colour transition. In particular, the response of the PDA‐ZnO−CE paper in several other organic solvents was poor as no transitions were observed hence its selectivity towards dimethylamine. In conclusion, the incorporation of PDA‐ZnO on cellulose paper is a step forward towards designing of a stimuli responsive packaging material that can detect biogenic amines released during food decomposition thereby preventing food poisoning.

Photocatalytic/sorption-self-cleaning activity of cellulose decorated with TiO2 and M@TiO2 (M=Au, Ag) polymeric nanocomposites

Titanium oxide nanoparticles (TiO2 NPs) are a semiconductor material widely employed as photocatalysts for environmental remediation owing to its excellent properties. Nevertheless, collecting the nanomaterial once dispersed in the aqueous media is challenging, while the photocatalytic activity is limited mainly to the ultraviolet range of radiation. In this work, we have modified cellulose paper, a sustainable and green support, with a polymer nanocomposite comprising nylon-6 and different nanomaterials, i.e., anatase TiO2 nanoparticles (NPs) as well as TiO2 decorated with Ag and Au in form of NPs by means of a simple procedure. The immobilization of the nanocomposite on paper mediated the subsequent recovery of the substrate upon incubation. The presence of nylon-6 enables both the attachment of the NPs on the support as well as the isolation of the pollutant from the contaminated water due to the interactions with the target analyte, i.e., methyl orange (MO). Additionally, the presence of the mentioned polyamide within the substrate triggers the photocatalytic reaction under visible light radiation. The broadening in the range of the light towards the use of sunlight has been also evaluated via modification of the photocatalyst nanoparticles with noble metals such as silver and gold. The kinetic of degradation of MO upon sunlight exposure with the different polymeric nanocomposites followed a pseudo-first-order model, with k constant values of 0.070, 0.083 and 0.120 min−1 for TiO2, Ag@TiO2 and Au@TiO2 nanocomposites, respectively. The effect of the presence of the polymer on the substrate has been evaluated, observing an increase in the k constant upon addition of the polyamide from 0.036 to 0.069 min−1 for TiO2. The synergistic effect of sorption/degradation enables the regeneration of the substrates modified with the nanomaterials that can be reused several times, the relative standard deviation of k upon three subsequent photocatalytic cycles being in the range 15.7–37.7%.

Cellulose nanowhiskers‐reinforced polymer nanofibers for photoresponsive authentication

AbstractThe objective of the current study is to develop novel photochromic polyurethane (PUR) nanofibrous films supported with cellulose nanowhiskers (CNW) and immobilized with nanoparticles of alkaline‐earth doped aluminate (NAEA) using the highly efficient and low‐cost solution blowing spinning (SBS) technique. CNW revealed a crystal diameter of 4–8 nm, and a crystal length of 55–105 nm. The solution blown spun nanofibers exhibited diameters of 250–450 nm. In order to prepare a transparent film, CNW and NAEA must be dispersed efficiently in the PUR composite. When supported with CNW, the efficiency of PUR nanofibrous films was strengthened. Cellulose paper sheets were coated with the colorless NAEA/CNW@PUR films to emit a green light at 518 nm upon excitation at 365 nm as proved by photoluminescence spectra. The prepared nanofibrous films exhibited efficient optical photochromic characteristics for potential security encoding applications. The nanofibers‐coated papers showed high photochromic reversibility without fatigue. The current approach can be reported as an efficient technology for authentication of commercial products.

Phosphorylated/amine-impregnated cellulosic paper for direct CO2 capture

A scalable papermaking process was employed herein to manufacture cellulosic papers from native and phosphorylated cellulose microfibers (referred to as CMF and PCMF, respectively) impregnated with polyethyleneimine (PEI) for Direct Air Capture (DAC) applications. These papers were analyzed in terms of their physico-chemical properties using several techniques. The impact of PEI content on desorbing the co-adsorbed H2O and CO2 from the air, as well as on the anisotropic microporous network, was explicitly analyzed. The results indicated that phosphorylation promotes the uptake of both CO2 and H2O in the corresponding neat and PEI-loaded papers, reaching a superior CO2 adsorption capacity of ∼0.7–0.9 mmol.g−1 for PCMF papers versus 0.07–0.3 mmol.g−1 for CMF papers. Furthermore, the CMF and PCMF papers exhibited H2O adsorption capacities in the range of 1.5–1.8 mmol.g−1 and 2.2–3.8 mmol.g−1, respectively. This work further highlights the combined role of phosphorylation and favorable PEI impregnation in tuning the cellulose CO2 adsorption properties under humid conditions, facilitating the rapid release of the adsorbed CO2 under mid conditions.

An all paper based triboelectric nanogenerators with high output performance in extreme environment manufactured by multi-layer papers forming technology

Triboelectric nanogenerators (TENGs) are regarded as a promising technology to drive the development of flexible/wearable electronics and self-powering sensor. Application of cellulose paper as the triboelectric positive materials makes TENGs more environmentally friendly. However, the limited output performance and stability in harsh environments and oxidation and corrosion of the metal electrodes have limited the practical application of cellulose paper based triboelectric nanogenerators (CPTENGs). Here, we have integrated cellulose paper-based triboelectric material and electrode in one sheet by using multi-layer forming technology in paper industry; the upper triboelectric layer shows excellent triboelectric positive performance, hydrophobicity and acid and alkali resistance, while the bottom electrode exhibits promise conductivity. The all CPTENGs can yield a maximum open-circuit voltage (VOC) of 227.1 V, a short-circuit current (ISC) of 6.9 μA. Furthermore, the VOC values of the all CPTENGs increase from 0.02 V to 225.1 V at the load resistance of 100 Ω∼10 GΩ; and a power density of 520 mW·m−2 is also obtained at a load resistance of 30 MΩ. Moreover, the VOC of CPTENGs not only retains up to 78 % of its initial value at a high relative humidity of 90 %, but also almost maintains unchanged in a wide range of the pH environment (pH = 1∼13). More importantly, the CPTENGs can be readily matched with paper-based zinc supercapacitor (P-ZISC) to act as an all paper based self-charging power system (PSCPS). The PSCPS is capable of driving various miniaturized electronics, such as electronic watch, temperature/humidity indicator, demonstrating its potential application in a sustainable power source for portable and green electronics.

Modifying cellulose fibres with carbon dots: a promising approach for the development of antimicrobial fibres.

This study focuses on the development of antimicrobial fibres for use in medical and healthcare textile industries. Carbon dots (CDs) were designed with boronic acid groups for the attachment to cellulose fibres found in cotton textiles and to enhance their attachment to glycogens on bacterial surfaces. Boronic acid-based and curcumin-based CDs were prepared and characterized using various techniques, showing a nanoscale size and zeta potential values. The CDs inhibited the growth of both Staphylococcus epidermidis and Escherichia coli bacteria, with UV-activated CDs demonstrating improved antibacterial activity. The antimicrobial activity of the CDs was then tested, revealing strong adherence to cellulose paper fibres with no CD diffusion and potent inhibition of bacterial growth. Cytotoxicity assays on human cell lines showed no toxicity towards cells at concentrations of up to 100 µg ml-1 but exhibited increased toxicity at concentrations exceeding 1000 µg ml-1. However, CD-modified cellulose paper fibres showed no toxicity against human cell lines, highlighting the antimicrobial properties of the CD-modified cellulose fibres are safe for human use. These findings show promising potential for applications in both industrial and clinical settings.

Antibacterial biocomposites: efficacy of MWCNT-coated Hanji cellulose paper against E. coli

Antibacterial biocomposites: efficacy of MWCNT-coated Hanji cellulose paper against E. coli

Development of Intelligent Indicators Based on Cellulose and Prunus domestica Extracted Anthocyanins for Monitoring the Freshness of Packaged Chicken.

Meat is a widely consumed food globally; however, variations in storage conditions along its supply chain can pose a potential food safety risk for consumers. Addressing this concern, we have developed freshness indicators designed to monitor the condition of packaged chicken. In this study, anthocyanins were infused with cellulose paper measuring 2 × 2 cm, and subsequent analysis focused on examining color changes concerning deteriorating chicken stored at 30°C for 48 h, with varying sample sizes being considered. The rise in total volatile nitrogen (TVB-N) compounds from an initial value of 3.64 ± 0.39 mg/100 g to 28.17 ± 1.46 mg/100 g acted as the stimulus for the color change in the indicator, simultaneously influencing the pH from the initial 7.03 ± 0.16 to 8.12 ± 0.39. The microbial load (aerobic plate count) of the chicken samples was also significantly increased. This collective shift in various parameters strongly suggests the occurrence of spoilage in chicken meat. The pH indicators exhibited a dark pink to red color for fresh chicken. As the chicken meat turned towards spoilage, the indicators changed to a dark blue and then a pale green color. FTIR spectroscopy results confirmed the presence of cellulose and anthocyanins. The FTIR analysis also validated the immobilization of plum anthocyanins within the cellulose paper and assessed their stability after 8 months of storage. Notably, the indicators demonstrated rapid sensitivity, showing a 20.5% response within one minute of ammonia exposure, which further increased to 29.5% after 3 min of exposure. The total color difference (ΔE) steadily rose in all the examined samples and also under various storage conditions. Overall, the indicators developed in this study exhibited a highly pronounced color transition, capable of distinguishing between fresh and spoiled chicken samples depending on the extent of spoilage and the specific day of observation.