Search

This article presents green in situ synthesis of ZnO directly on polyethylene terephthalate (PET) fabrics using pomegranate peel extract. The surface of PET was activated by environmentally friendly oxygen plasma, and the process was compared to alkali treatment where the extract of wood ash was used instead of classical chemicals. Sorption analysis showed that the hydrophilic character of the plasma-treated sample was much better than that of the alkali-treated and untreated samples. Both treatments slightly decreased the breaking strength and elongation of the fabric. Scanning electron microscopy, colour measurements, dispersive X-ray spectroscopy, and antioxidant activity investigations showed that the ZnO particles were successfully synthesised on alkali- and plasma-treated PET. The liquid chromatography-mass spectrometry results showed that ellagic acid and punicalagin were the most abundant compounds in the pomegranate peel extract that enabled the synthesis of ZnO. The UV protection, amount of ZnO, and uniformity were the highest for the ZnO prepared on the PET samples by the plasma-assisted green synthesis. Additional optical assessment of fabric porosity and thickness measurements confirmed that these fabrics have excellent UV protection due to the presence of ZnO.

The development of durable multifunctional properties is crucial for the production of high-performance technical textiles. In this work, a novel, environmentally friendly and facile method was developed for the chemical modification of cotton fabric by in situ biosynthesis of Ag NPs in the presence of sumac leaf extract as a reducing agent on TiO

The development of cellulose-based textiles that are functionalised with silver nanoparticles (AgNP), synthesised according to a green approach, and offer protection against ultraviolet (UV) radiation and pathogenic bacteria is very important today. In the present work we demonstrate the environmentally friendly approach to obtain such textile material by AgNP synthesis directly (in-situ) on cotton fabrics, using water extracts of plant food waste (green tea leaves, avocado seed and pomegranate peel) and alien invasive plants (Japanese knotweed rhizome, goldenrod flowers and staghorn sumac fruit) as reducing agents. The extracts were analysed for their total content of phenols and flavonoids and their antioxidant activity. The synthesised AgNP on cotton were round, of different size and amount depending on the reducing agent used. The highest amount of AgNP was found for samples where Japanese knotweed rhizome extract was used as reducing agent and the lowest where extracts of goldenrod flowers and green tea leaves were used. Regardless of the reducing agent used to form AgNP, all cotton samples showed excellent protection againstE. coliandS. aureusbacteria and against UV radiation with UV protection factor values above 50. The best results for UV protection even after the twelve repetitive washing cycles were found for the sample functionalized with AgNP synthesised with an extract of the Japanese knotweed rhizome. Due to the presence of AgNP on cotton, the air permeability and thermal conductivity decreased. AgNP had no effect on the change in breaking strength or elongation of fabrics.Graphic abstract

This research presents a new procedure for the chemical modification of cotton fabric, which included a ‘’green’’ in situ synthesis of silver particles using an extract of sumac leaves as a reducing agent. To increase the adsorption ability of silver cations, a sol-gel matrix was previously created on cotton fabric using an organic–inorganic precursor sol-gel. The presence of silver particles on the cotton fabric was confirmed by scanning electron microscopy and energy-dispersive X-ray spectroscopy. The results showed that silver particles were created on the cotton fabric in the presence of the sumac leaf extract, which colored the fibers in brown. The presence of the sol-gel matrix increased the adsorption of silver cations and therefore the concentration of sliver particles, which resulted in a deeper color yield. Silver particles provided antibacterial protection, with a 99–100% reduction of E. coli in S. aureus bacteria, while the sumac leaf extract provided excellent protection against ultraviolet radiation, with an ultraviolet protective factor equaling 66.54. The coating was also highly durable in terms of its washing fastness.

This work examines the possibility of using leaves from the invasive plant species Fallopia japonica (Japanese knotweed) as a source of dye for the natural dyeing of cotton. To achieve a higher uptake of extracted dye, a cationic agent instead of a classical mordant was used to treat the cotton prior to dyeing. Distilled water and 0.5 M NaOH were used as extraction mediums to produce natural dyebaths with different concentrations (10, 20 and 50 g/L) of Fallopia japonica leaves. The colorimetric measurements revealed that a higher concentration of extract, the extraction of leaves in NaOH and a cationic pretreatment of cotton yield a dark-brown-coloured cotton with good wash stability.

Technical textile materials with multifunctional protective properties represent one of the largest and fast growing segments of the textile industry. Multifunctional water- and oil-repellent and flame-retardant coating on polyester (PES) fabric was prepared in this research using fluoroalkyl-functional siloxane (FAS) as the water- and oil-repellent finishing agent and organophosphonate (OP) as the flame-retardant agent. A finishing solution containing FAS and OP of appropriate concentrations was applied to the untreated and oxygen plasma-treated PES fabric samples using the pad-dry-cure method. For comparison, single-component FAS and OP finishing solutions were applied to the fabric samples under the same conditions. The coated PES samples were washed under standard conditions. The morphological, chemical and functional properties of the coated PES samples were determined with scanning electron microscopy, Fourier transform infrared spectroscopy, wet pick up, liquid contact and sliding angles measurements as well as oil repellence and vertical burning tests. The results reveal that oxygen plasma treatment prior to finishing significantly increased the wettability of the PES fibres, which directly resulted in increased concentration of the absorbed finishing agents. This treatment enabled the creation of PES fabric with simultaneous uperhydrophobic, oleophobic and flame-retardant properties. Although the superhydrophobic and oil-repellent characteristics of the coating were preserved after washing, the flame retardancy was hindered because of the removal of OP in the washing bath.

This study presents an eco-friendly protocol for the hydrophilization of polyethylene terephthalate (PET) fabric and the in situ synthesis of ZnO particles. The alkaline medium and reducing agent for ZnO synthesis were prepared as aqueous extracts from wood ash and pomegranate peel, respectively. Due to the hydrophobic nature of the PET fabric, oxygen plasma treatment was included in the process. The influence of plasma treatment in different synthesis steps on the formation of ZnO and consequently on the morphological, colour and ultraviolet (UV) protective properties of the samples was discussed. The study showed that incorporating oxygen plasma treatment before immersing the samples in each solution for the ZnO in situ synthesis (natural alkaline medium of wood ash, zinc salt and natural reducing agent from pomegranate peel) produced PET fabric with the most uniform ZnO layer without visible cracks and the highest UV-blocking ability with a UV protection factor (UPF) of 300+. The colour measurements showed that increasing the number of plasma treatments leads to higher colour strength of the samples. Herein, a novel protocol for the production of protective PET fabrics is presented, which is also an example of a completely environmentally benign textile functionalization process.

This work presents two protocols for the green in situ synthesis of zinc oxide nanoparticles (ZnO-NP) on cotton with the aim to develop sustainable cotton fabric with an ultraviolet protection factor (UPF). The protocols differed in the order of immersing cotton fabric in reactive solutions of three batches, i.e., precursor (0.1 M zinc acetate dihydrate), reducing agent (aqueous extract of Japanese knotweed leaves) and alkali (wood ash waste). The scanning electron microscope (SEM) results showed that ZnO-NP were successfully synthesised on cotton using both protocols; however, only the protocol where cotton was first immersed in alkali, then in the precursor and, lastly, in the reducing agent enabled very high UPF and higher amount of Zn present on the sample. Due to the different order of cotton fabric immersion in the reactive solutions, dissimilar morphology of the ZnO particles was observed, which resulted in different UV blocking abilities of the samples. The antioxidant analysis (DPPH) showed that the natural reducing agent prepared from Japanese knotweed leaves has very high antioxidant activity, which is attributed to phenolic compounds present in the plant. The reflectance spectroscopy results confirmed that the colour yield and colour of the samples did not influence the UPF value. This protocol is an example of green circular economy where waste materials of invasive alien plant species and pellet heating was used as a natural source of phytochemicals, for the direct synthesis of ZnO-NP to develop cotton fabric with UV-protective properties.

The influence of the treatment process on the dyeability of cotton fabric with a natural dye from goldenrod blooms was studied in this research. The dyeing was performed on untreated and treated cotton samples. The treating of the samples, using mordant (KAl(SO4)2 × 12 H2O), was performed before and during the dyeing process, whilst treatment with a cationic agent (Denimcol FIX-OS) was performed only before dyeing. The dyeing was carried out at 60 °C in two repetitions in three different concentrations of goldenrod aqueous extract, namely without dilution, and by diluting the extract with distilled water at volume ratios of 1:2 and 1:3. Spectrophotometric measurements were done before and after 1, 5, and 10 washing cycles. Colour fastness to rubbing was visually evaluated using a grey scale. Colour fastness to artificial light was visually evaluated using a blue scale, as well as spectrophotometrically before and after illumination of the dyed samples. The results of the research show that the cationic treatment of cotton fabric essentially influences on higher dye uptake in comparison to treatment using mordant before or during dyeing. Cotton samples that are treated with a cationic agent have the highest colour fastness to washing, rubbing, and light among all of the studied samples.

This paper presents an in-depth study of the surface modification of polyethylene terephthalate fabric (PET) with non-thermal plasma and temperature- and pH-responsive nanogel (PNCS) to impart smart thermoregulation properties. To increase the adsorption of the PNCS nanogel onto the PET, ammonia and oxygen plasma and a combination of both plasma gases were used. Chemical changes caused by the plasma treatment were investigated using X-ray photoelectron spectroscopy (XPS), morphological changes were determined using scanning electron microscopy (SEM) and the swelling and de-swelling ability was determined by measuring the moisture content at 20 and 40 °C. The greatest deposition of the PNCS nanogel, with unimpaired swelling ability, was found on the oxygen-plasma-treated samples, as they had the highest O/C ratio. Meanwhile, the least promising results were found for the samples treated with a combination of oxygen and ammonia plasma, where the highest concentration of nitrogen was present on the fibre surface. Since the treatment with oxygen plasma proved to be the most effective method, different exposure times to the oxygen plasma, namely, 10, 30 and 60 s, were studied in the second part of this study. The optimal oxygen plasma treatment time was found to be 30 s, where the greatest deposition and unhindered swelling/de-swelling ability of the PNCS nanogel on the PET fabric was achieved.

A new functional, stimuli-responsive microgel coating on polyamide 6 (PA6) fabric with simultaneous temperature (T)- and pH-responsive moisture management, UV protection and photocatalytic self-cleaning properties was prepared by applying poly-(N-isopropylacrylamide)/chitosan (PNCS) microgel in combination with ZnO nanoparticles to PA6 fabric. Two different application procedures were used: (i) the application of PNCS previously functionalized with a ZnO nanoparticles suspension and (ii) the application of PNCS with the subsequent application of a ZnO nanoparticles suspension. The coatings were fabricated on the untreated PA6 fabric as well as on fabric previously modified by the silica matrix created by the sol-gel precursor iSys MTX in order to increase the adsorption ability and uniformity of the coating. The chemical and morphological properties of the coated PA6 samples were determined by SEM and FTIR analyses. Stimuli responsiveness and functional properties were assessed by the moisture content, water vapour transmission rate, water uptake, UV protection and photocatalytic self-cleaning measurements. The results show that the application procedure as well as the pretreatment of PA6 fabric greatly infl uenced the properties of the coating. Accordingly, the most appropriate procedure included the creation of a silica matrix on the PA6 fibres followed by the application of PNCS and subsequent application of ZnO. In this case, the modified PA6 fabric exhibited high T and pH responsiveness due to the swelling/de-swelling activity of the PNCS microgel, as well as good UV protection with UPF equal to 18.8 and photocatalytic self-cleaning properties that are even higher than those in the case of the one-component coating with ZnO.

This work presents the novel and entirely green in situ synthesis of zinc oxide nanoparticles (ZnO-NP) on cotton fabric. Pomegranate peel extract was used as a reducing agent and wood ash extract was used as an alkali source for the formation of ZnO-NP from zinc acetate. Four different synthesis methods, which varied in drying between immersion of fabric in the active solutions for synthesis and the use of padding and ultrasonication, were investigated to evaluate the most suitable one to achieve excellent ultraviolet (UV) protective properties of the functionalized textile. For comparison, the cotton fabrics were also functionalized with each active solution separately or in a combination of two (i.e., Zn-acetate and plant extract). Scanning electron microscopy (SEM), inductively coupled plasma mass spectroscopy (ICP-MS), Fourier transform infrared spectroscopy (FTIR), X-ray diffractometry (XRD) analysis, and atomic force microscopy (AFM) confirm the successful formation of ZnO-NP on cotton. Among the synthesis methods, the method that included continuous drying of the samples between immersion in the active solutions for synthesis (Method 4) was found to be the most suitable to deliver uniformly impregnated cotton fibers with numerous small ZnO wurtzite structured crystals and excellent UV protection, with a UV protection factor of 154.0. This research presents an example of a green circular economy where a bio-waste material can be used to produce ZnO-NP directly on cotton at low temperatures and short treatment times without the addition of chemicals and enables the production of cellulosic fabrics with excellent UV protection.

Polyethylene terephthalate (PET) fabric was treated in a late afterglow of plasma created by a microwave (MW) discharge in the surfatron mode, by using oxygen (O2) and ammonia (NH3) gases. The series of treatments using one gas or the combination of both at different treatment times were performed in order to increase the embedment of UV-responsive microcapsules that were deposited onto PET with pad-dry-cure process. Plasma in both gases was characterized by optical emission spectroscopy (OES), which showed substantial dissociation of O2 and NH3 molecules as well as formation of NHx radicals due to the partial dissociation of ammonia molecules. The chemically active species in the plasma afterglow changed the surface properties of PET that were analysed using X-ray photoelectron spectroscopy (XPS), time-of-flight secondary ion mass spectrometry (ToF–SIMS), Fourier transform infrared spectroscopy (FTIR), scanning electron microscopy (SEM) and water absorption analysis. The effectiveness of plasma treatment on embedment of UV-responsive microcapsules on PET was evaluated by UV-responsiveness, colour strength and colour depth using reflectance spectroscopy, add-on and air permeability, respectively. Treating PET by O2 afterglow followed by a longer treatment by NH3 afterglow increased the polymers hydrophilicity and concentration of nitrogen-rich functional groups on surface that enabled higher uptake of UV-responsive microcapsules, and consequently better responsiveness of fabric to UV radiation. The add-on of microcapsules was almost 8-times higher and the colour depth increased up to 75% for plasma treated samples.

Dyeing of raw and bleached cotton fabrics with a natural dye of curcumin was studied to implement the ancient and environmentally friendly technique of developing photos called anthotype. With the aim of achieving diff erent colours of dyed cotton fabrics, several modifi cations were performed, such as extraction of curcumin in hard and soft water, after-treatments of dyed cotton, i.e. with ferrous sulphate, zinc chloride and silver nitrate, aftertreatment in alkaline bath, and aftertreatment with other natural dyes (blueberry and raspberry). The colour values of dyed samples were determined using a refl ectance spectrophotometer. Colour stability to light was determined by the standard method in Xenotest. It was found that the use of various metal salts, natural dyes, alkalinity and hardness of water infl uenced the colour changes of the substrate. Yellow, red, greenish and brownish colours of fabrics were produced by diff erent treatments. Since the use of metal ions improved the stability of curcumin to light, the motifs produced by anthotype technique were hardly visible. It was found that the natural dye of blueberries and raspberries did not infl uence the light stability, therefore a larger colour contrast between exposed and unexposed areas of the fabric was visible, and consequently good visibility of the motifs was achieved.

The high-performance fibrous polymers are incorporated in products for specific uses where have to perform exceptionally (i.e. high strength, stiffness, heat resistance and/or chemical resistance). The lack of certain functional groups and high crystallinity of high-performance fibrous polymers decrease their adhesion when used in a matrix. One of the most promising and environmentally benign methods to overcome these the drawbacks is plasma technology. The chapter reviews the contemporary research on the topic. The plasma surface modifications, such as cleaning, physical etching, chemical modification, and polymerization on glass, aramid, carbon, polyethylene and poly(p-phenylene benzobisoxazole) fibrous polymers are discussed.

Oxygen plasma pre-treatment was applied to cotton fabric with the aim of improving the water repellency performance of an inorganic-organic hybrid sol-gel perfluoroalkyl-functionalized polysilsesquioxane coating. Cotton fabric was pre-treated with low-pressure oxygen plasma for different treatment times and operating powers. Afterward, 1H,1H,2H,2H-perfluorooctyltriethoxysilane (SiF) was applied to the cotton fabric samples using the pad-dry-cure method. The surfaces of the untreated and modified cotton fibers were characterised using Fourier transform infrared spectroscopy, Xray photoelectron spectroscopy, scanning electron microscopy, and atomic force microscopy. The water repellency of the SiF-coated fabric samples was evaluated using static and sliding contact angle measurements with water. The results show that the plasma treatment with the shortest treatment time (10 s) and the lowest operating current (0.3 A) increased the atomic oxygen/carbon ratio of the cotton fiber surface from 0.6 to 0.8 and induced the formation of a nano-sized grainy surface. Increasing the plasma treatment time and/or operating current did not intensify the surface changes of the cotton fibers. Such saturation effects were explained by the large influence of reactive oxygen atoms during the plasma treatment. The measured static water contact angles on the surface of the untreated and plasma pre-treated and SiF-coated cotton fabrics showed that the oxygen plasma pre-treatment enabled the increase of the water contact angle from 135° to ≈150°, regardless of the applied plasma treatment time and discharge power. This improvement in the hydrophobicity of the SiF coating was followed by a decrease in the sliding angle of water droplets by more than 10° compared to the plasma untreated and SiF-coated sample characterized by a water sliding angle of 45°. Additionally, measurements of the water sliding angle revealed that the increase of the static contact angle from 149° to 150° corresponded to a drop of the water sliding angle from 33 to 24°, which suggests that the plasma pre-treatment of 20 s at an operating current of 0.3 A produced the best water-repellent performance of the SiF-coated cotton fabric.

To achieve colourful and antibacterial textiles using ecologically friendly processes, cotton and bamboo rayon knitted fabrics were treated using radio-frequency low-pressure water vapour plasma and dyed with the extract of Fallopia japonica (Japanese knotweed) rhizome. Optical emission spectroscopy (OES) was used to observe plasma during the sample treatment and scanning electron microscopy (SEM) to study morphological changes of samples. The adsorption of F. japonica on cellulose substrates was studied by measuring the colour (CIE L*a*b*) and colour yield (K/S) of dyed samples. The antibacterial properties against Escherichia coli and Staphylococcus aureus were tested as well. The results show that water vapour plasma induces weak etching effect on the surface of the cellulose samples, since water molecules in plasma dissociate to produce hydroxyl radicals and oxygen atoms. Plasma-treated samples had higher dye uptake, and better antibacterial properties against S. aureus. The samples did not have antibacterial properties against E. coli.

The cellulose fabrics made from 100 % cotton with antibacterial and UV protective properties were successfully created by loading of Ag/TiO2 nanocomposite during and after dyeing with yellow, red and blue reactive dye. Blank dyeing (dyeing with all chemicals except dye) was performed to show that reactive dyes have an ability to increase the adsorption and adhesion of Ag/TiO2 nanocomposite on cotton fabrics. The colour of the samples before and after washing and exposure to artificial light was measured by reflectance spectroscopy. The presence of nanocomposite on samples was confirmed by scanning electron microscope. The increased adsorption capacity of cotton towards Ag/TiO2 nanocomposite due to the presence of reactive dyes was confirmed by measuring the quantity of silver using inductively coupled plasma mass spectroscopy. The same samples showed excellent UV protective properties with UV protection factor (UPF 50+), and excellent antibacterial properties against E. coli and S. aureus. Due to a good adhesion of nanocomposite on samples where loading of nanocomposite and dyeing with reactive dye was performed simultaneously, the samples retained their excellent protective properties after repetitive washing cycles.

The development of lignocellulosic natural-fibre-reinforced polymers composites are constrained by two limitations: the upper temperature at which the fibre can be processed and the significant differences between the surface energy of the fibre and the polymer matrix. Since the fibres and matrices are chemically different, strong adhesion at their interface is needed for the effective transfer of stress and bond distribution throughout the interface. The present study investigated the plasma induced effects on the surface properties of natural coir fibres. Weakly ionized oxygen plasma was created in two different discharge chambers by an inductively coupled radiofrequency (RF) discharge. The water absorption studies showed an increase of water sorption from 39% to 100%. The morphological study using scanning electron microscopy (SEM) analysis also confirmed the surface changes which were observed after the plasma treatment. The topographic measurements and phase imaging done using atomic force microscopy (AFM) indicated difference in topographic features and etching of coir wall, which points to the removal of the first layer of coir fibre. X-ray photoelectron spectroscopy (XPS) analysis revealed that the oxygen content measured for samples treated at 50 Pa increased from initial 18% to about 32%.

Raw cotton fabrics have been exposed to low-pressure non-equilibrium gaseous plasma to improve the adsorption of natural dyes as well as ultraviolet (UV) protection factor. Plasma created in a glass tube by an electrodeless radiofrequency (RF) discharge was created either in oxygen or ammonia at the pressure of 50 Pa to stimulate formation of oxygen and nitrogen groups, respectively. The type and concentration of functional groups was determined by X-ray photoelectron spectroscopy (XPS) and morphological modifications by scanning electron microscopy (SEM). The colour yield for curcumin dye was improved significantly for samples treated with ammonia plasma what was explained by bonding of the dye to surface of amino groups. Contrary, the yield decreased when oxygen plasma treatment was applied due to the negatively charged surface that repels the negatively charged dye molecules. The effect was even more pronounced when using green tea extract as the colouring agent. The colour difference between the untreated and ammonia plasma treated sample increased linearly with plasma treatment time reaching the factor of 3.5 for treatment time of 300 s. The ultraviolet protection factor (UPF) was over 50 indicating excellent protection due to improved adsorption of the dye on the ammonia plasma treated samples.

Low-pressure oxygen plasma created by an electrodeless radiofrequency (RF) discharge was applied to modify the properties of cellulosic fibrous polymer (cotton) in order to improve adsorption properties towards zinc oxide (ZnO) nanoparticles and to achieve excellent ultraviolet (UV) protective properties of cotton fabric. The chemical and physical surface modifications of plasma-treated cotton fabric were examined by X-ray photoelectron spectroscopy (XPS) and scanning electron microscopy (SEM). The mechanical properties of plasma-treated samples were evaluated, measuring strength and elongation of the fabrics. The quantity of zinc on the ZnO-functionalized cotton samples was determined using inductively coupled plasma mass spectrometry (ICP-MS) and the effectiveness of plasma treatment for UV protective properties of cotton fabrics was evaluated using UV-VIS spectrometry, measuring the UV protection factor (UPF). The results indicated that longer plasma treatment times cause higher concentration of oxygen functional groups on the surface of fibres and higher surface roughness of fibres. These two conditions are crucial in increasing the content of ZnO nanoparticles on the fibres, providing excellent UV protective properties of treated cotton, with UPF factor up to 65.93.

Weakly ionised gaseous plasma created in a moist tetrafluoromethane gas at a low pressure with an electrodeless radiofrequency discharge was applied to modify the surface properties of cellulose fibres. The plasma was used to increase the adsorption of zinc oxide (ZnO) nanoparticles such that cellulose fibres with good ultraviolet (UV) protective properties could be created. The UV protection factor (UPF) values of the ZnO-functionalised fibres were determined as a function of the plasma treatment time. The chemical and physical surface properties of the plasma-treated fibres were examined using scanning electron microscopy, X-ray photoelectron spectroscopy, and wettability tests. The quantity of zinc on the fibres was determined using inductively coupled plasma mass spectroscopy. The results indicated that 30 s of plasma treatment resulted in ZnO-functionalised samples with lower UPF values than samples without plasma treatment due to the creation of fluorine-rich functional groups on cellulose fibres and the agglomeration of ZnO nanoparticles. The highest UPF values (50+) were obtained when samples were treated with plasma for 10 s. These high UPF values were a result of the increased adsorption of uniformly distributed ZnO nanoparticles caused by fibres surface functionalization and roughening upon plasma treatment. Furthermore, the mechanical properties of textiles treated with moist CF4 plasma for 10 s were slightly improved.

Surface morphology of woven cotton fabrics was modified by treatment with mild plasma created in tetrafluoromethane (CF4) at the pressure of 60 Pa. Samples of dimensions 20 cm × 20 cm were mounted into a 27-cm-wide cylindrical plasma reactor powered with a radio frequency generator of frequency 27.12 MHz and output power of about 500 W. The volume of the reactor was 17 l and the corresponding power density was solely 30 W/l. The plasma density was estimated with a double electrical probe and was about 2 × 109 cm−3. The type of radicals created in plasma was determined using optical emission spectroscopy (OES). No CFx and a negligible amount of F radicals were observed by OES, and surprisingly the predominant spectral features were CO bands. The evolution of surface morphology vs. plasma treatment time was monitored by scanning electron microscopy. Originally smooth fibers became extremely rough after prolonged treatment. The results were explained by etching of fibers with gases released from the samples ...

The use of ZnO for the functionalization of textile substrates is growing rapidly, since it can provide unique multifunctional properties, such as photocatalytic self-cleaning, antimicrobial activity, UV protection, flame retardancy, thermal insulation and moisture management, hydrophobicity, and electrical conductivity. This paper aims to review the recent progress in the fabrication of ZnO-functionalized textiles, with an emphasis on understanding the specificity and mechanisms of ZnO action that impart individual properties to the textile fibers. The most common synthesis and application processes of ZnO to textile substrates are summarized. The influence of ZnO concentration, particle size and shape on ZnO functionality is presented. The importance of doping and coupling procedures to enhance ZnO performance is highlighted. The need to use binding and seeding agents to increase the durability of ZnO coatings is expressed. In addition to functional properties, the cytotoxicity of ZnO coatings is also discussed. Future directions in the use of ZnO for textile functionalization are identified as well.

The surface modification of cellulose fibres was performed with the use of low-pressure water vapour plasma, followed by the application of a pad-dry-cure sol-gel coating with the water- and oil-repellent organic-inorganic hybrid precursor fluoroalkyl-functional siloxane (FAS), with the aim of creating the “lotus effect” on the cotton fabric surface. The tailored “lotus effect” was confirmed by measurements of the contact angle of water (154°) and n-hexadecane (140°), as well as by measurements of the water sliding angle (7°), which were used to identify the super-hydrophobic, oleophobic and self-cleaning properties of the modified fibres. The chemical and morphological changes caused by modifications of the fibres were investigated by XPS, FTIR, AFM and SEM. The results show that the plasma pre-treatment simultaneously increased the surface polarity, average roughness, and surface area of the fabric. The application of the FAS coating after plasma pre-treatment caused only a slight increase in the surface roughness, accompanied by a decrease in the surface area, indicating that the architecture of the surface was significantly changed. This result suggests that the surface pattern affected the “lotus effect” more than the average surface roughness. The plasma pre-treatment increased the effective concentration of the FAS network on the fabric, which resulted in enhanced repellency before and after repetitive washing, compared with that of the FAS-coated fabric sample without the plasma pre-treatment. Despite the fact that the plasma pre-treatment increased the concentration of the oxygen-containing functional groups on the fabric surface, this phenomenon insignificantly contributed to the adhesion ability and, consequently, the washing fastness of the FAS coating.

Bleached, mercerized cotton fabrics were used in this research. In the first phase, the dyeing of cotton fabrics with a blue vat dye Bezathren Blau BCE was performed, and in the second phase, the dyed fabrics were immersed into a colloidal silver solution. The colloidal silver solution was prepared via synthesis from AgNO3 and reduced with NaBH4. Parent cotton fabrics were also immersed into the colloidal silver solution. A comparison of the quantity of silver on the parent and vat-dyed cotton fabrics was performed. Inductively coupled plasma mass spectrometry revealed a silver content that was almost two times higher on the dyed and silver-treated cotton fabrics. All samples (parent and dyed) treated in the colloidal silver solution showed excellent antimicrobial activity. The fiber surfaces were imaged using a scanning electron microscope. The mechanical properties of vat-dyed and vat-dyed silver-treated fabrics and the wash fastness of silver-treated samples were determined.

In an attempt to use minimal concentrations, initially, of silver nanoparticles for loading onto textiles and to achieve maximum concentrations on the material, CF4 low-pressure plasma was used on bleached and mercerized cotton fabric. The concentrations of silver on the fabrics were determined by the ICP-MS method (inductively coupled plasma-mass spectrometry), the morphology of fiber surfaces was observed with a scanning electron microscope (SEM), and an x-ray photoelectron spectroscopy (XPS) study was used for the evaluation of surface chemical changes. The antibacterial effect of silver loaded fabrics was tested against Enterococcus faecalis and Pseudomonas aeruginosa. The best results were found for plasma-treated cotton fabric functionalized with 30 nm silver particles. The results show effective plasma etching of the fabric surface, which caused excellent adhesion of silver particles. Color measurements of dyed samples showed that CF 4 plasma does not affect the color of dyed cotton. The mechanical properties of cotton remain unaltered after plasma treatment.

The objective of this research was to use Ar/N2 (50%:50%) plasma to increase the adhesion of nano silver particles to raw polyester fabric. RUCO-BAC AGP was applied using the exhaust method. X-ray photoelectron spectroscopy revealed differences in surface composition between the Ar/N2 plasma-treated and untreated raw fabrics. The Ar/N2 plasma treatment was found to increase the surface carbon concentration and decrease the concentration of C-O and O-C=O groups on the surface. After plasma etching, the specific surface of the polyester fabric and properties related to it were found to change significantly. This change was confirmed by a decrease in the whiteness index and an increase in the dyeability of the polyester fabric with disperse dye. Morphological changes in the surface of plasma-treated polyester fabric enabled greater adhesion of nano silver particles and increased the antimicrobial effect with respect to Pseudomonas aeruginosa, Escherichia coli and Streptococcus faecalis.

In this work, the antibacterial and other properties of polyester fabrics previously functionalized by corona and/or silver nano particles have been studied. Corona air plasma was used as a pretreatment of raw, washed and washed-thermostabilized polyester fabrics to increase the adhesion of nano silver particles resulting in an excellent antibacterial effect. X-ray photoelectron spectroscopy was applied to analyze the surface composition and chemical bonding of the surface atoms on untreated and treated fabrics. The surface morphological changes of polyester fibers were observed by scanning electron microscopy (SEM). The quantity of silver on the polyester fabrics was determined by the use of the inductively coupled plasma-atomic emission spectrometry method. The antimicrobial properties of functionalized polyester fabrics were tested according to American Society for Testing and Materials ASTM Designation: E 2149-01. Additionally, the dyeing of polyester fabrics with selected disperse dye as well as capillary action tests were performed to confirm the chemical and morphological changes of polyester fibers after corona treatment. Considerable differences in surface composition were found between the raw and washed or washed-thermostabilized fabrics. The surface of raw fabrics is richer in carbon and the concentrations of the C—O and O—C=O groups are lower than on the other samples. An opposite effect is observed for washed and washed thermostabilized fabrics. SEM analyses show that the plasma treatment also affects the surface morphology. The chemical surface composition and morphology are highly related to the hydrophobicity and hydrophylicity, and the achievement of better nano silver adhesion and enhanced dyeing and antimicrobial properties of differently prepared corona plasma-treated polyester fabrics. Therefore, corona air-treated raw polyester fabrics demonstrated optimum antimicrobial properties due to the excellent adhesion of nano silver.

The purpose of this research was to determine the influence of temperature, pH, and the addition of sodium oxide silicium oxide (soso) on the dyeability of cotton warp during the process of dip-dyeing. A simulation of the dip-dyeing technique was used. The results show a negligible influence of dip-dyeing bath temperature on the color yield of cotton warp. Lower pH values of dip-dyeing baths cause better dyeability. Addition of soso has a particular influence on the color yield of cotton warp. As a result, the dip-dyeing procedure is shortened when soso is used. The change of color of dip-dyed cotton warp, depending on different pH of the baths and on the addition of soso, was studied using x-ray diffraction (XRD) and scanning electron microscopy (SEM) analyses. XRD showed that the dyeing conditions do not affect the crystallographic form of indigo, which is form B in all cases. On the other hand, SEM revealed the reasons for the observed effects in the differences in the morphology of the indigo crystallites.

The influence of different application methods on UV protective properties of white and dyed cotton functionalized with ZnO nanoparticles (nano-ZnO) was investigated. The methods differ in application procedure, time of treatment and auxiliaries used in the treating bath. The ultraviolet protection factor (UPF) was determined for untreated and functionalized samples. The presence of nano-ZnO on fibres was investigated using scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR). The content of Zn was determined with energy-dispersive X-ray spectroscopy (EDS) and inductively coupled plasma mass spectrometry (ICP-MS). Dynamic light scattering (DLS) was used for particle size measurements in the prepared solutions. The results show that UV protection of cotton increases with a higher content and uniform distribution of nano-ZnO on the samples and that dyeing increases the loading capacity of cotton towards nano-ZnO. One of the methods (Method IV) gave remarkable results giving cotton an excellent UV protection whether it was dyed or not.

Samples of bleached cellulose fabric were treated with weakly ionized highly dissociated oxygen plasma in order to improve the binding of ZnO nanoparticles, antibacterial properties and biodegradability. Low specific discharge power of about 24 W l−1 was applied in order to minimize thermal effects following plasma treatment. Optical emission spectroscopy revealed weak etching of the fabric while x-ray photoelectron spectroscopy showed formation of oxygen-rich functional groups. Scanning electron microscopy revealed an improved uptake of ZnO nanoparticles and the standard transfer method highlighted excellent antimicrobial effects for Staphylococcus aureus and Escherichia coli. The biodegradability of all samples was determined using the standard ISO test and revealed excellent results for plasma-treated samples even in cases when they were functionalized using ZnO nanoparticles.

Some applications of extremely non-equilibrium oxygen plasma for tailoring the surface properties of organic as well as inorganic materials are presented. Plasma of low or moderate ionization fraction and very high dissociation fraction is created by high frequency electrodeless discharges created in chambers made from a material of low recombination coefficient. The O atom density often exceeds 1021 m−3 which allows for rapid functionalization of carbon-containing materials. Surface saturation with polar oxygen-rich groups is achieved in a fraction of a second and further exposure leads to etching. The etching is often non-uniform and results in nano-structuring of surface morphology. A combination of rich morphology and saturation with polar functional groups allows for a super-hydrophilic character of originally hydrophobic materials. Polymer composites are etched selectively so the polymer component is removed from the sample surface, leading to modified surface properties. Furthermore, such a treatment allows for distinguishing the distribution and orientation of fillers inside the polymer matrix. The exposure of inorganic materials to non-equilibrium oxygen plasma causes one-dimensional growth of metal oxide nanoparticles, thus representing a unique technique for the rapid catalyser-free growth of nanowires.