Preparation of cellulose-based electrospun fluorescent nanofibres doped with perylene encapsulated in silica nanoparticles for potential flexible electronics.

Novel fluorescent nanofibres were developed via the electrospinning of chromophore-doped cellulose. Two different perylene-doped cellulose fluorescent fibres were fabricated using cellulose as a host material and perylene dye derivatives as active dopants. Fluorescent cellulose nanofibres were prepared via the electrospinning technique using two different perylene dyes, including perylene diimide and perylene mono-imide sodium/potassium salts. The generated fluorescent silica nanoparticles exhibited diameters varying in the range 80-180 nm. The generated electrospun fluorescent nanofibrous structures displayed smooth surfaces with average diameters of 200-300 nm for cellulose comprising perylene diimide and sodium/potassium salts of perylene mono-imide dyes, respectively, dispersed uniformly in the cellulose matrix. The generated fluorescent nanoparticles and nanofibres were characterized by different standard methods, including scanning electron microscopy (SEM), transmission electron microscopy (TEM), fluorescent optical microscope (FOM) and Fourier-transform infrared spectra (FT-IR). The fluorescence properties of the fabricated cellulose nanofibres were explored. Those fluorescent nanofibres pave the way for the development of promising textile fluorescence materials, such as flexible displays, photonics, and optical devices.

Enhancement of the Functional Performance of Cotton and Polyester Fabrics upon Treatment with Polymeric Materials Having Different Functional Groups in the Presence of Different Metal Nanoparticles.

This work examined the functional properties of three different treated fabrics, cotton, polyester, and cotton/polyester, with different polymeric materials (polyvinyl alcohol (PVA), carboxymethyl cellulose (CMC), or chitosan) in the presence and absence of two synthesized metal nanoparticles to impart and enhance fabric properties. Both metal nanoparticles (silver nanoparticle (AgNPs) and Zinc oxide nanoparticles (ZnONPs)) were synthesized using Psidium guajava Leaves and characterized using different techniques. The different treated fabrics were dyed with Reactive Dye (Syozol red k-3BS) and evaluated for their color strength, fastness properties, ultraviolet protection, antimicrobial activity, and mechanical properties. Results showed that treatment with polyvinyl alcohol (PVA), carboxymethyl cellulose (CMC), or chitosan enhances the functionality of all fabrics, with improved color strength, UV protection, and antimicrobial properties. Additionally, mechanical properties were slightly increased due to the creation of a thin film on the fabric surface. All dyed treated fabrics showed good ultraviolet protection and antimicrobial properties. The K/S of all treated textiles including nanoparticles and polymers was marginally greater than that of the treated materials without polymers. The UPF values demonstrate that the three investigated polymers and both metal nanoparticles enhance the fabrics' ability to block UV radiation and shield people's skin from its damaging effects. All treated textiles had UPF values that are higher than those of untreated textiles. Further research demonstrates that ZnONP-treated textiles exhibited greater UPF values than AgNP-treated textiles when the polymer component was present. Antibacterial examination demonstrated that treated materials had robust microbial resistance. This resistance is diminished by washing, but still prevents bacterial growth more effectively than untreated textiles.

Preparation of cellulose gel extracted from rice straw and its application for metal ion removal from aqueous solutions.

Rice straw waste was used to extract natural cellulose fibers, which was then chemically converted to cellulose gel. Both extracted cellulose and modified cellulose (gel) were characterized using different techniques and used for biosorption of b+arium, manganese, cobalt, nickel, copper, zinc, and cadmium. Both celluloses' chemical compositions were investigated. The FT-IR, XRD, TEM, and SEM results all support the success of the proposed chemical modification. Because of the increase in pore size within the gel composition, the metal sorption capability of the final chelating material (gel) was greater than that of extracted cellulose. The experimental data were fit to the sorption isotherm models of Langmuir, Freundlich, and Temkin. This new modified biopolymer's behaviour suggested that it could be used as a promising sorbent for cation removal from polluted dye baths and waste water. Furthermore, this modified cellulose was prepared as cheap material extracted from the rise waste which helping in protection of the environment and it was confirm excellent behaviour in the removal heavy metals from their aqueous solution compared to the previous materials reported before.

Controllable Release of Povidone-Iodine from Networked Pectin@Carboxymethyl Pullulan Hydrogel.

Povidone-iodine (PI) is a common antiseptic reagent which is used for skin infections and wound healing. The control release of PI is quite important to heal the deep and intense wounds. Herein, the preparation of biodegradable pectin@carboxymethyl pullulan (Pe@CMP) hydrogel was carried out and applied for controllable release of PI. CMP was synthesized by interaction of monochloroacetic acid with pullulan at different ratios. The Pe@CMP hydrogel was then prepared by crosslinking of pectin with CMP in presence of glutaraldehyde as cross linker. After carboxymethylation, COOH contents were enlarged to be 24.2-51.2 mmol/kg and degree of substitution was 0.44-0.93. The rheological properties of Pe@CMP hydrogel were enlarged by increment of pectin ratio. Swelling ratio in water (16.0-18.0%) was higher than that of artificial sweat (11.7-13.2%). Pe@CMP hydrogel containing 20% pectin, exhibited the lowest release and 57.7% from PI was released within 360 min. The biological activity of the released PI was monitored to be highly efficient. The kinetic of release was fitted well to the first ordered reaction and Higuchi models. The mechanism of release was explained by the swelling of hydrogel. The networked structure of hydrogel was opened by swelling and PI was released from the outer pores followed by inner pores, achieving the controllable release.

Cellulosic fabric treated with hyperbranched polyethyleneimine derivatives for improving antibacterial, dyeing, pH and thermo-responsive performance.

Having cotton fabrics with multifunctional properties is of the most research focused on using either different processes or new and different materials. Improving thermo - responsive and antibacterial properties of cotton fabrics decorated with silver nanoparticles and nanogel has been investigated. During this research silver nanoparticles (AgNPs) have been in situ prepared using poly(N-isopropyl acrylamide)/polyethyleneimine microgel. Prepared particles have been characterized, visualized their morphological structure and their particle through microscopic analysis, which proved that their particle size was in range of (6-10 nm). The decorated gel with silver nanoparticles has been functionalized with silicone compounds to produce hybrid material. The produced gel has been characterized for its pH, temperature, textural, rheological, antimicrobial, cytotoxicity, and conductivity properties. The functional properties of the treated and untreated fabrics have been investigated, and the results proved that treated fabric has conductivity, antibacterial, pH and thermo-responsive properties.

Multifarious cellulosic through innovation of highly sustainable composites based on Moringa and other natural precursors.

Innovative composites processed using sorted out and characterized precursors from nature were formulated, synthesized then applied to cotton cellulose in the fabric form to confer on the cellulose multifunctional performance properties. Precursors embrace Moringa oleifera leaves aqueous and alcoholic extracts, chitosan, clay known as Kaolin and, silver nanoparticles (AgNPs). The latter were prepared under the reducing and stabilization actions of Moringa extracts. These Precursors are mixed to form binary or tertiary mixture formulations under variable formation conditions of the required composites. The composites and fabrics treated thereof were submitted to characterization, analysis and testing using traditional tools as well as state-of-the-art facilities including FT-IR, UV, Particle size analyser, TEM, SEM and EDX. Aqueous and alcoholic Moringa extracts exhibit different chemical attributes meanwhile both extracts fail to induce formation of AgNPs at up to pH 6. Intensive formation of AgNPs occurs only with the alcoholic extract provided that pH 8 or higher was employed. The particle size of AgNPs decreases by increasing the pH indicating chemical combination of Moringa extract and chitosan Moringa aqueous or alcoholic extract exhibit larger particle size than those containing chitosan and AgNPs. AgNPs were characterized by spherical shape with precise distribution of the particles. The nitrogen content, the physical properties and the mechanical properties of the treated fabrics were taken to demonstrate the magnitudes of intercalation and interactions of Moringa aqueous and alcoholic extracts individually and in composite with the cellulosic fabric. It was as well to emphasize the high antimicrobial activity imparted by current composites to the cellulosic fabrics. Equal emphasis was placed on UPF and easy-care properties of the treated fabrics. To this end, current research brings into focus novel cellulosic products with multifunctional performance as a direct impact of multifarious attributes caused by chemical combination of the composite in question and cellulosic fabrics.

Colchicine mesoporous silica nanoparticles/hydrogel composite loaded cotton patches as a new encapsulator system for transdermal osteoarthritis management.

Colchicine is a drug from the past with a bright shining future. It has gained much attention nowadays due to the newly explored therapeutic avenues that were opened by its application in serious ailments. Colchicine has been recently observed as a potential treatment for osteoarthritis (OA). OA is a widespread joint degenerative disease that causes extensive pain and disability. Colchicine has been discovered to affect bone turnover and to reduce different cytokines like interleukin 6 (IL6). Colchicine oral administration has several limitations including extensive first-pass effect, poor bioavailability, and severe GIT side effects. The transdermal route circumvents these limitations. However, colchicine transdermal delivery is challenging owing to its high aqueous solubility and hence poor skin permeation. In this study, novel colchicine transdermal delivery systems were developed to conquer such obstacles. Cellulose-based patches were primed, where mesoporous silica nanoparticles (MSNs) were prepared and used as colchicine encapsulators. The free colchicine or the encapsulated drug was embedded into self-healing hydrogel. The hydrogel was prepared by reacting carboxyethyl chitosan and oxidized pullulan. These composites were used to treat cotton fabric to produce easily applicable and extended-release transdermal patches. Nitrogen adsorption-desorption isotherms, DLS, TEM, and SEM were used to estimate surface area, pore-volume, size, zeta potential, and morphology of MSNs. The hydrogel was characterized using FTIR and TEM. The prepared cotton patch was tested for fabric stiffness. Ex vivo drug permeation study through isolated rat skin was conducted. In comparison to free drug aqueous solution, the patches revealed enhanced drug flux and amplified permeated drug levels which were sustained all over 24 h. Skin permeation was further validated via confocal laser microscopy using fluorescein. The therapeutic investigation of colchicine formulated patches in mono-iodoacetate (MIA)-induced rat osteoarthritis model depicted improved locomotor activity, glutathione blood level, and remarkable decline in levels of malondialdehyde, nitric oxide, TNF-α, and COX-2. Histopathology of rats knee joint supported the OA protective effect of the developed patches, The obtained results revealed significant potentiality of the developed colchicine mesoporous silica nanoparticles/hydrogel patches in the offering, efficient safe and patient convenient formulation for OA management.

Hydrogel bioink based on clickable cellulose derivatives: Synthesis, characterization and in vitro assessment.

Hydrogel is considered as a promising candidate for bioink in terms of biocompatibility, biodegradability, printability and supporting cellular behavior. Recently, carbohydrates derivatives containing alkyne and azide pendant functional groups have been used in medical applications due to their improved chemical, biological, functional properties, and their amenability for chemical reactions under mild conditions. In this work, a novel bioink was developed based on azide and alkyne of cellulose derivatives. Azido-hydroxyethyl cellulose (D.Sazido = 0.04) was synthesized via open-ring reaction of 1-azido-2,3-epoxypropane and characterized spectroscopically and titrimetrically. Alkyne derivative, propargyl carboxymethyl cellulose (D.Spropargyl = 1.72) was synthesized through coupling reaction with propargylamine in the presence of EDC and NHS. The click-gel scaffold was obtained by mixing the two novel candidates in the presence of copper (I) catalyst. Extrusion bio-plotting experiment was successfully conducted of the two solutions into coagulant Cu (I)/DMSO solutions and demonstrated the possibility of using the clickable cellulose derivatives as bioink precursors. Chemical and physical properties of the click-gel were demonstrated. The biocompatibility assay of the prepared click-gels showed high level of viability in the human skin fibroblast cells (HFB4) at concentration 100 µg/mL.

Development of multifunctional modified cotton fabric with tri-component nanoparticles of silver, copper and zinc oxide.

A facile method, cost-effective and highly efficient with shortened-time operation was devised for unprecedented modification of cotton fabrics. This modification induced the formation of metallic and metal oxide nanoparticles within cotton fabrics in such a way that cotton samples loaded with AgNPs- or AgNPs/ZnONPs or AgNPs/ZnONPs/CuNPs respectively. Presence of the trimetallic nanoparticles concomitantly within microstructural features of cotton imparts durable antibacterial, UV protection and conductivity properties to yield ultimately cotton fabrics with multifunctional performance. The nanoparticles were formed and stabilized independently by Polymethylol compound (PMC) and functionalized polyethyleneimine (FPEI) as per one bath. The results obtained proved that the solution of these metal compounds are turned from colourless to yellow and black green colour up on addition of PMC or FPEI compound. It was found that UV-vis spectra display maximum surface plasmon peak of around 410-415 confirming the successful synthesis of AgNPs stabilized by PMC or FPEI chains. In addition, the results obtained indicated that the as formed nanoparticles are successfully deposited into the surface of cellulose fabrics and reveal changes in crystalline structure. Fabrics underwent structural changes during their treatments as per the designed practice exhibit multifunctional properties and manifold performance. The resultant treated cotton fabric gives good antibacterial properties event after 20 washing cycles additionally to the excellent ultra-violet properties and excellent electrical conductivity.

Enhancement the thermo-regulating property of cellulosic fabric using encapsulated paraffins in modified pectin.

Synthesis of smart hosting materials from solvent free modified pectin with fatty acid (have different molecular weight) have been occurred and characterised. Modified pectin with phase change material (PCM) have been prepared and applied to textile material. Smart composite matrix based on modified pectin was produce thermo-regulating characteristics which play the main role to control body temperature for various daily wear. The microcapsules (pectin/PCM) and treated fabric were characterized using SEM, DSC and FT-IR. The results confirmed the synthesis of modified pectin using solvent free method, and also confirmed its reaction with cotton surface. DSC result confirmed that, the treated fabrics have a thermo-regulating property.

Benign development of cotton with antibacterial activity and metal sorpability through introduction amino triazole moieties and AgNPs in cotton structure pre-treated with periodate.

The research work presented herein was undertaken with a view to develop, characterize and highlight modified cotton fabrics that acquire durable antibacterial activity in concomitant with high metal sorption capacity. The development is based on reacting cotton cellulose previously oxidized by sodium periodate-with 4 amino-1,2,4 triazole in presence and absence of silver nano particles (AgNPs). The idea behind the periodate pretreatment is to convert (via oxidative cleavge) the 2,3-vicinal diol of the anhydroglucose units of cotton into aldehyde groups. The latter are easily reacting with the triazole groups in the modified cotton. On the other hand AgNPs were fabricated as per the reduction method using bio-material extracted from the root of licorice. By virtue of its reducing action, the bio-material converts Ag+ ions to Ag0 atom which is also stabilized Ag the bio-material in the form of cluster which is the agregate of about 5 Ag0. The clusters are cropped with the stabilizer thus forming silver nanoparticles. Measurement of the particle size displays a value of 8.7nm. Charactrisation of triazole treated cotton fabrics reveals the presence of the triazole moieties inside the structure of cotton. Furthermore, Fabrictreated with triazole in presence and absence of AgNPs exhibits a relatively high antibacterial activity against gram-negative tested bacteria (E. coli) as compared to that of gram-positive tested bacteria (S. aureus). The metal sorption of triazole treated cotton fabrics was higher than those of untreated or periodate pretreated fabric due to the increase in nitrogen centers created along the cellulose chains. Experimental data were accomplished through Langmuir, Freundlich and Temkin sorption isotherm models. It was shown that sorption follows Langmuir isotherm model and suggests that the innovative fabric in question can adsorb metal ions from polluted dye bath.

Laminating of chemically modified silan based nanosols for advanced functionalization of cotton textiles.

As per to silver nanoparticles/silicon dioxide nanoparticles (SiO2@AgNPs) properties (e.g., conductivity, reactant, adsorption, detachment and antimicrobial), many researchers were focused on its preparation technique. A core/shell of silicon dioxide and silver nanoparticles (SiO2@AgNPs) has been prepared by facile route. The as synthesized core/shell nanoparticles were chemically modified with two different silan compounds, nominated, vinyltriethoxysilan (VTEOS) and (3-aminopropyl)trimethoxysilan (APTEOS). World class facilities such as XRD, FT-IR, TEM, Particle size, DLS, SEM techniques were utilized for the nanoparticles characterization. The nanoparticulate system comprises SiO2@AgNPs, SiO2@AgNPs/APTEOS were applied to cotton fabric using butantetracarboxylic acid (BTCA) as across-linking agent. While UV irradiation by photo initiator was used as crosslinking agent for SiO2@AgNPs/VTEOS on cotton fabrics. The Treated cotton fabrics were evaluated for their surface morphology and heat transfer ability as well as antibacterial activity. The obtained data prove that the core/shell was successfully prepared, with AgNPs in core. In addition, both silan compounds (APTEOS, VTEOS) were successfully reacted with the outer shell SiO2. The results declared also that the treated fabrics exhibit a good antibacterial activity as well as good thermal properties.

Surface modification of SiO2 coated ZnO nanoparticles for multifunctional cotton fabrics.

A simple chemical synthetic route was designed to prepare zinc oxide nanoparticles (ZnO-NPs) by using sodium alginate as anti-agglomeration agent in the presence of sodium hydroxide as alkali. Next, surface modification of ZnO-NPs with SiO2 nanoparticles was achieved as per to sol-gel process. Further enhancing of the multifunctional properties of SiO2@ZnO-NPs was conducted successfully thanks to (aminopropyl)triethoxysilan (APTES) and vinyltriethoxysilan (VTES) which, in turns, increase the affinity of the SiO2@ZnO-NPs nanocomposite towards glycosidic chains of cotton fabrics. Thorough characterizations of synthesized ZnO-NPs, SiO2@ZnO-NPs, SiO2@ZnO-NPs/APTES and SiO2@ZnO-NPs/VTES were conducted by the making use of well advanced techniques such as FT-IR, XRD, TEM, DLS and SEM-EDX. The data obtained clarified the formation of an interfacial chemical bond between ZnO and SiO2 as affirmed by FT-IR and XRD analysis. In addition, the results revealed by TEM, zeta sizer and SEM-EDX techniques, declared that the amorphous layers of SiO2, APTES or VTES evenly coated the surface of ZnO-NPs. For these nanocomposites, the work was extended to render cotton fabrics multifunctional properties such as antibacterial and UV protection with high durability even after 20 washing cycles using pad dry cure method. Taking the advantages of the silane compounds terminated by active groups such as OH, NH2, etc., open the door for further functionalization of the cotton fabrics' surfaces by durable multifunctional agents applied in various applications.

Enhancement of flame retardancy and water repellency properties of cotton fabrics using silanol based nano composites.

Environmental concerns related to fluorinated and organophosphorus compounds led to a consideration of the methods for imparting flame retardancy and water/oil repellency to textiles. A simple and facile method for fabricating the cotton fabric with superhydrophobicity and flame retardancy is described in the present work. Complex coating with amino-functionalized silica nano-particles on epoxy-functionalized cotton accompanied with ZnO nano-particles coating are carried out. In This context, new preparation techniques were used to prepare both aminated silica and ZnO nano-particles. The particle size was investigated using Transition Electron Microscope (TEM) and the chemical structure was investigated using FT-IR analysis and other analytical techniques. Cotton was functionalized with epoxy and carboxyl via grafting cotton with nano-emulsion consisted of mixture of glycidyl methacrylate (GMA) and acrylic acid (AA), and then treated for functional finishing through conventional pad-dry-cure method. The treated fabrics showed good water repellency and excellent flame retardant properties as determined by the standard test methods.

Supercritical carbon dioxide assisted silicon based finishing of cellulosic fabric: a novel approach.

Usage of supercritical carbon dioxide as a medium for finishing cotton fabrics with modified dimethylsiloxane polymers terminated with silanol groups was investigated, different cross-linkers namely 3-isocyanatepropyltriethoxysilane (IPES) and tetraethylorthosilicate (TEOS) were used for covalently bonding between silicon and cellulose. The presence and the amount of PDMS compounds on the treated fabrics were characterized by FT-IR. Qualitative and quantitative information on the distribution of the silicon molecules across the fibre cross section was provided by SEM/EDX analysis and Confocal Raman microscopy (CRM) respectively. The results confirm that all fibres treated with PDMS and IPES have larger silicon amounts than those treated with TEOS. SC-CO2 medium provides good coating of cotton surface with a 3D network of DMS compound and cross linker, and leads to forming highest DMS concentration in a layer between 1 and 2µ under the surface of cotton fabrics.

Suitability of Confocal Raman microscopy for monitoring the penetration of PDMS compounds into cotton fibres.

PDMS compound was chosen as a molecule-model for investigating the diffusion of silicon products into cotton bulk. The study demonstrates the suitability of Confocal Raman microscopy (CRM) to monitor the distribution of poly(dimethylsiloxane) (PDMS) molecules into cotton fibres. Different molecular weights of PDMS compounds were used in two different solvents (water and hexane) at various temperatures (25, 50 and 60°C). The surfaces of the fibres were studied with scanning electron microscopy and Confocal Raman microscopy was run to detect the PDMS on the surface and in the bulk of treated fabrics. We concluded that all PDMS compounds, irrespectively their molecular weights and the silicon oil infiltrate into cotton fibre. The penetration is strongly dependent on the solvent used. Water proved suitable for assisting the infiltration of low and medium molecular weight PDMS, at elevated temperatures. High molecular weight PDMS infiltrates better from hexane and at room temperature than from water.