Introduction

The development of innovative textile materials aims to endow them with multifunctional properties (Foksowicz-Flaczyk et al. 2016). Several functions in one material are also expected in the area of textronic products called electronic textiles (E-textiles). Such products connect textiles and electronics and can be relevant for the development of smart materials capable of achieving a broad spectrum of functions, e.g., in flexible electronic products (Stoppa and Chiolerio 2014; Gowri et al. 2010). E-textile products have many applications, e.g., in biomedical sensors (electrocardiogram sensors), piezoresistive sensors, piezoelectric materials (optical resonator and transducer), rehabilitation (electromagnetic shields in physiotherapy) as well as professional sports and recreation (smart suits) (Rattfalt et al. 2007; Zhou et al. 2014; Capineri 2014; Usma et al. 2015; Dias 2015). Modifiers such as silver, carbon, gold and copper are the most common conductors and can be combined with various textile materials using conventional and unconventional methods (Cieślak et al. 2009; Stempien et al. 2016; Shateri-Khalilabad and Yazdanshenas 2013; Cui et al. 2015). In the last decade, much research has been dedicated to conductive textiles obtained by the application of carbon nanotubes (Kowalczyk et al. 2015; Nasirizadeh et al. 2015; Makowski et al. 2015), graphene, graphene oxide (Shateri-Khalilabad and Yazdanshenas 2013; Shen et al. 2016), carbon nanotubes and graphene oxide nanocomposites (Tang et al. 2014) or conductive polymers such as polypyrrole (Nateghi et al. 2013; Kim et al. 2013) and polyaniline (Zhao et al. 2013; Agarwal et al. 2016) and conductive polymers such as PEDOT/PSS (Tarabella et al. 2012). Silver has many excellent properties, including conductivity (Johnsen et al. 2012), good catalytic performance and antimicrobial activity (Jiang et al. 2005). The application of silver in the form of silver nanowires (AgNWs) is important in electronics as well as opto-electronic and nanoelectromechanic devices because of the unique properties, which are not seen in three-dimensional materials (Nateghi and Shateri-Khalilabad 2015). The application of AgNWs to modify textile substrates enables obtaining multifunctional products. Additionally, the combination of AgNWs, e.g., with photocatalysts, gives new opportunities to obtain functional materials with high potential for applications (Eom et al. 2014; Dong et al. 2014). With the development of wearable devices and electronic textiles, there will be increasing development of electrically conducting pathways produced using conventional fiber and yarn substrates. The methods of deposition, spinning, printing, coating, dipping and solution growing to obtain conductive materials have been widely used (Cui et al. 2015).

The aim of this article was to develop electroconductive and antibacterial cotton (natural fibers) and viscose (chemical fibers) fabrics by modification with an AgNW colloid. The obtained modification effect, impact of AgNW application on fabrics' tensile strength and durability of AgNW layers on fabric surfaces were assessed.

Materials and methods

Preparation of AgNW colloids

AgNWs were synthesized by a polyol process in which silver nitrate (AgNO3, Aldrich) was reduced with ethylene glycol (EG, POCH) in the presence of polyvinylpyrrolidone (PVP, Aldrich). PVP is an amorphous polymer, which is highly soluble in polar solvents, that directs the growth of nanowires and protects them from agglomeration (Xia and Sun 2002; Mohd et al. 2014; Shobin and Manivannan 2014; Sun et al. 2002). Briefly, 10 ml of 0.45 M EG solution of PVP (M w = 55 000) with 7 mg of sodium chloride (NaCl, CHEMPUR) was prepared and heated to 170 °C. Chloride ions were added as the mediating agent to facilitate the growth of AgNWs. Then, 5 ml of 0.12 M EG solution of AgNO3 was injected at a rate of 5 ml/h. During the synthesis, the solution was magnetically stirred. When the silver precursor solution was added, the colloid was heated for 60 min at 170 °C and finally air-cooled to about 22 °C. To remove EG and excess PVP from the colloid, the solution was diluted with acetone (POCH) (at a 1:10 ratio) and centrifuged for 10 min. Finally, the nanowires were dispersed in ethanol (POCH) to form the 0.5 wt% alcoholic colloid.

Deposition of AgNW colloid on fabric surfaces

The samples of 100% cotton (108 g/m2, pick and end densities—warp 43 and weft 32) and 100% viscose (104 g/m2, pick and end densities—warp 32 and weft 25) plain woven fabrics were dipped in the AgNW colloid for 1 min, and then the fabrics were dried at room temperature for 30 min (dipping and drying method). This method was used 1 and 10 times (for cotton fabric) and 1, 10 and 15 times (for viscose fabric) to vary the AgNW content on the fabrics. The AgNW content on cotton after 1 dipping was 1 g/m2 and after 10 dippings 9 g/m2; for viscose after 1 dipping it was 0.9 g/m2, after 10 dippings 6.2 g/m2 and after 15 dippings 8.4 g/m2.

Methods

The optical absorbance spectra of AgNW colloids were obtained using an Ocean Optics USB2000+ spectrophotometer and ethanol as the reference. Microscopic analysis of AgNWs deposited on the carbon-coated copper grids was performed using a scanning transmission electron microscope (STEM) (Nova NanoSEM 450 FEI, USA). Microscopic analyses of unmodified cotton fabric (CO) and viscose fabric (CV) and AgNW-modified fabrics were carried out with a scanning electron microscope (SEM) (Nova NanoSEM 450 FEI, USA, and Vega 3 Tescan, Czech Republic). The elemental composition analysis was made with an X-ray microanalyzer (INCA Energy EDX, Oxford Instruments Analytical, UK) connected to a Vega 3 SEM. Alicona MeX software for 3D SEM images of modified fabrics was used. On the basis of the 3D SEM analysis, the values of the average height of the selected area (S a), root-mean-square height of the selected area (S q) and maximum height of the selected area (S z) were determined. Surface resistance (R s) of unmodified and AgNW-modified fabrics was evaluated according to standard PN-P-04871:1991. The measurements were carried out with a set of standardized measurement electrodes, a digital DM53 multimeter (Polmed(+), Poland) and 6206 teraohmmeter (ELTEX, Germany). The fabrics were tested in an air-conditioned HCZ 0030 L(M) chamber (Heraeus, Germany) at a temperature of 23 ± 1 °C and relative humidity of 25 ± 5%. Before testing, samples were conditioned under the same conditions for 24 h. FTIR/ATR spectra of unmodified and modified fabrics and PVP powder were recorded with 4 cm−1 resolution over the range 600–4400 cm−1 using a Vertex 70 FTIR spectrometer (Bruker, Germany). Raman spectra of the AgNW colloid (after drying) and fabrics were obtained with a Raman Renishaw InVia Reflex with a Leica microscope (Renishaw, GB), and a near-infrared semiconductor laser (λ = 785 nm) was used as an excitation source. The laser beam was focused on the samples by a 50× objective lens. Laser power and scanning times were determined experimentally. The signal was recorded by a CCD detector. Spectra were baseline corrected using WIRE 3.2. software. The X-ray diffraction technique (XRD) on an Empyrean diffractometer (PANalytical), working in grazing incidence (GIXRD) with Co kA (1.78901 A) mode radiation to measure the AgNW colloid and fabrics, was used. The incidence angle (omega) was set to 2°. The thermogravimetric analysis of the PVP powder, AgNW colloid (after drying) and fabrics was carried out using a TG 209F1 Libra analyzer (Netzsch, Germany) with a heating rate of 10 °C min−1 under a nitrogen flow rate of 20 ml min−1 over the range of 30–800 °C. The fabric samples at about 6 mg and the dry residue of the AgNW colloid at about 2 mg were tested in a ceramic crucible. Further data processing was done using the ICDD PDF 4 database and HighScore Plus software. The washing durability of AgNW-modified fabrics was evaluated according to standard PN EN ISO 6330:2012. The Ag percentage weight in AgNW-modified fabrics before and after washing was evaluated on the basis maps collected from 100 µm × 100 µm surfaces using the SEM/EDX technique. As a complementary technique, TG/DTG analysis was used. The abrasion resistance of AgNWs on both fabric surfaces using Stainingtester (Hungary) was examined. A pin diameter of 10 mm and press force of 9 Pa were used. Twenty abrasion cycles were carried out. Tensile strength tests before and after fabric modification were performed according to standard PN-EN ISO 13934-1:2013-07 using an Instron 3367 Tensile Test Machine (UK). The breaking force and breaking elongation values were determined. The antibacterial activity of AgNW-modified CO fabric was studied according to the AATCC 100-2004 and PN-EN ISO 20743 standards using Staphylococcus aureus (S. aureus, ATCC 6538, gram-positive bacterium) and Klebsiella pneumoniae (K. pneumoniae, ATCC 4352, gram-negative bacterium) as model microorganisms. Approximately 0.6 × 105 and 1.8 × 105 per ml (CFU/ml) colony-forming S. aureus and K. pneumoniae were inoculated, respectively. Inhibition zones were measured after 21 h + 48 h of incubation at 37 ± 2 °C.

Results and discussion

AgNW colloid

For characterization of the AgNW colloid used in the modification of fabrics, UV–Vis spectroscopy and microscopy analyses were used. Figure 1 shows the absorption spectrum taken from the as-prepared AgNW colloid. The appearance of a peak at 350 nm can be attributed to the plasmon response of the long silver nanowires similar to that of the bulk silver. The absorption peak at around 380 nm can be considered the transverse mode of AgNWs (Sun et al. 2002; Wang et al. 2005).

Fig. 1
figure 1

UV–Vis spectrum of AgNW colloid

Full size image

STEM images of synthesized AgNWs at different magnifications are shown in Fig. 2. The silver nanowires (AgNWs) are homogeneous in morphology and not agglomerated. The nanowire diameters were 46 ± 2 nm.

Fig. 2
figure 2

STEM image of AgNWs with ×50,000 and ×250,000 magnifications

Full size image

Conductivity

AgNW-modified cotton and viscose fabrics change color from white to silver gray, which is consistent with literature reports (Cui et al. 2015; Nateghi and Shateri-Khalilabad 2015). The unmodified CO and CV fabrics are nonconductive, and their surface resistance amounted to 2.4 × 1012 and 8.9 × 1011, respectively (Table 1). After one dipping in the AgNW colloid, a few AgNWs were observed on CO1AgNW and CV1AgNW fabrics. The percentage weight of Ag on the basis of SEM/EDS analysis amounted to 3.8% (CO1AgNWs) and 1.4% (CV1AgNWs) (Figs. 3b, 4b), and the surface resistance (R s) decreased for CO1AgNWs by about two orders of magnitude and was not changed for CV1AgNWs (Table 1). After ten dippings of the CO fabric in the AgNW colloid, the Ag content was 53.3%; the fabric became conductive, and the R s value was 20 Ω (Fig. 3c; Table 1). For the CV fabric after ten dippings, the Ag content was 34.8%, and R s was 8.6 × 104 Ω (Fig. 4c; Table 1). The CV10AgNW fabric was also conductive, but the effect was worse compared to CO fabric. The electrical properties depend on electrically conductive paths formed by AgNWs. The increase in the amounts of AgNWs causes better interconnection between silver nanowires, which allows for good electrical conductivity. After 15 dippings, the CV fabric achieved high conductivity, and the R s amounted to 46 Ω (Ag content 52.3 wt%) (Fig. 4d; Table 1). In the same conditions, more effective AgNW modification of CO compared to the CV surface was observed. For further studies, we selected the best electrically conductive textiles: CO fabric after 10 dippings in AgNWs (CO10AgNWs) (Fig. 3c) and CV fabric after 15 dippings (CV15AgNWs) (Fig. 4d). The surface resistance of PET/CO woven fabric modified with carbon nanotubes was in the range of 5.79 × 103–1.03 × 103 Ω, respectively, from one to four paddings with nanotubes (Kowalczyk et al. 2015). Cui et al. (2015) examined the influence of the strain of cupro fabrics modified with AgNWs on electrical conductivity; low resistance and good stretchability in the range of 4.7–9.1 × 10−3 Ω in the strain range of 0–190% were obtained. Shen et al. (2016) obtained electrical cotton fabric dyeing with reduced graphene oxide. The lowest surface resistance was 1.43 × 103 Ω/cm at the seventh dyeing cycle. Tarabella et al. (2012) prepared conductive cotton fiber modified with functionalized poly(3,4-ethylenedioxythiophene) doped with poly(styrene sulfonate) (PEDOT:PSS) with electrical resistance of 4.3 × 102 Ω/cm.

Table 1 Surface resistance (R s) of unmodified and AgNW-modified CO and CV
Full size table
Fig. 3
figure 3

SEM/EDX analysis of a CO, b CO1AgNW and c CO10AgNW fabrics

Full size image
Fig. 4
figure 4

SEM/EDX analysis of a CV, b CV1AgNW, c CV10AgNW and d CV15AgNW fabrics

Full size image

Surface analysis

The 3D SEM pictures (Fig. 5) show the changes in the surface topography of fibers after AgNW deposition. To evaluate the changes in surface roughness of AgNW-modified fabrics, 3D SEM pictures were made. The 3D pictures of unmodified CO and CV fabric surfaces and the roughness parameters were shown by Giesz et al. (2016). Obtained by this research team, the value of the root-mean-square height in the selected area (S q) for unmodified CO and CV was 44 and 9 nm, respectively. The roughness of fabric surfaces after AgNW deposition was determined. The value of S q for the measured area of 64 µm2 was 197 and 216 nm for CO10AgNWs and CV15AgNWs, respectively. Other measured roughness parameters such as the average height S a increased from 33 nm (CO) to 155 nm (COAgNWs10) and from 7 nm (CV) to 171 nm (CV15AgNWs). The increase of maximum height S z before and after modification was also observed from 547 nm (CO) to 1.84 µm for CO10AgNWs and from 124 nm (CV) to 1.88 µm for CV15AgNWs.

Fig. 5
figure 5

Three-dimensional SEM pictures of a CO10AgNW and b CV15AgNW fabrics

Full size image

Vibrational spectroscopy techniques were used for the assessment of AgNW layers directly on the fabric surface. On the FTIR/ATR spectrum of PVP powder (Figs. 6, 7a), the band at 3419 cm−1 and four peaks with the maximum at 2952 cm−1 corresponded to –OH stretching and C–H stretching vibrations, respectively. The peak at 1647 cm−1 corresponded to the stretching vibrations of C=O in the PVP. Other peaks at 1281 and 1425 cm−1 referred to the C–N stretching vibration and the CH2 groups in the pyrrole ring of PVP (Selvam and Sundrarajan 2012). On the FTIR/ATR spectrum of CO10AgNW fabric, the broad band peak corresponding to –OH stretching shifted to a lower wave number from 3332 cm−1 (Fig. 6a, CO fabric) to 3286 cm−1 (Fig. 6b, CO10AgNW fabric). Also in the CV15AgNW fabric spectrum, the –OH stretching band shifted from 3333 cm−1 (Fig. 7a, CV fabric) to 3324 cm−1 (Fig. 7b, CV15AgNW fabric). The C=O stretching band of CO10AgNW fabric shifted from 1641 to 1648 cm−1 (Fig. 6a, b) and for CV15AgNW fabric shifted strongly from 1641 to 1688 cm−1 (Fig. 7a, b). These changes were evidence of the interaction among cellulose, PVP and silver nanowires. Sundarshan Reddy et al. (2012) examined hydroxypropyl cellulose (HPC) and PVP in aqueous solutions. On the basis of FTIR analysis, they found the formation of strong hydrogen bonds between HPC (–OH group) and PVP (C=O group) by the shift of absorption bands. Also, interaction between PVP and cotton was observed by Selvam and Sundrarajan (2012). Additionally, Hong et al. (2010) observed broadened and shifted C=O stretching bands of the silver/PVP nanocpomosite compared to the PVP powder band. This was associated with the formation of a coordination bond between the silver and oxygen atoms in the C=O group.

Fig. 6
figure 6

FTIR analysis of a CO fabric, b CO10AgNW fabric and c PVP powder

Full size image
Fig. 7
figure 7

FTIR analysis of a CV fabric, b CV15AgNW fabric and c PVP powder

Full size image

Raman analysis confirmed the FTIR/ATR analysis and additionally as a complementary technique showed a strong band at 239 cm−1 (Fig. 8c). As reported by Wang et al. (1999) and Martina et al. (2012), this vibration was characteristic for the Ag–O mode, silver's interaction with oxygen molecules. Bands from PVP at 746 cm−1 (C–N stretching vibrations), 938, 938 cm−1 (C–C stretching vibrations) (Fig. 8d) and 748, 937 cm−1 (Fig. 9d) in CO10AgNW and CV15AgNW fabrics, respectively, were noticed. The band at 1687 cm−1 for CV15AgNW fabric (Fig. 9d) was attributed to C=O stretching vibrations from PVP, and it was not observed for CO10AgNW fabric (Fig. 8d). On the Raman spectrum of CO10AgNW and CV15AgNW fabrics, bands at 1235 and 1428 cm−1 corresponded to C–N stretching and C–H bending vibrations of PVP, respectively (Bahadur et al. 2016). The presence of the above bands from PVP in the AgNW colloid spectrum was also observed (Figs. 8c, 9c).

Fig. 8
figure 8

Raman analysis of a PVP powder, b AgNW colloid, c CO fabric and d CO10AgNW fabric

Full size image
Fig. 9
figure 9

Raman analysis of a PVP powder, b AgNW colloid, c CV fabric and d CV15AgNW fabric

Full size image

The XRD results of CO10AgNW, CV15AgNW fabrics and AgNW colloid confirmed the presence of metallic silver on the fabric surface and in colloidal solution. The two diffraction peaks centered at two theta around at 44.59° (200) and 51.93° (002) are characteristic for silver. Other reflections at 26.87°, 40.80° and 22.57°, 25.54° corresponded to the crystal structure of CO and CV, respectively (Fig. 10).

Fig. 10
figure 10

XRD analysis of a AgNW colloid, b CO10AgNW and c CV15AgNW fabrics

Full size image

The Ag percentage weight on the surface in relation to other percentage weights of elements in the fabrics before and after washing was evaluated by the energy-dispersive X-ray spectroscopy technique. The Ag content before washing was 53.5 and 52.3% for CO10AgNW and CV15AgNW fabric, and the surface resistance was 20 and 46 Ω, respectively. After 25 washes (CO10AgNWs/25), the Ag content decreased by about 9 wt%, but the fabric still exhibited high conductivity; the surface resistance (R s) was 55 Ω (Fig. 11; Table 2). After 50 washes (CO10AgNWs/50), the Ag content decreased about 11 wt%, and R s was 195 Ω. It was found that after the first 25 washes, the Ag content decreased the most, while after the next 25 washes, it decreased slightly. For CV15AgNWs after the first (CV15AgNWs/1) and second washes (CV15AgNWs/2), the Ag content decreased from 52.3 to 13.3 wt% and 3.9 wt%, respectively. Therefore, the conductivity decreased, and after the second wash the CV15AgNWs/2 fabric was nonconductive. The loss of AgNWs as the result of washing was shown by SEM/EDS analysis (Fig. 11).

Fig. 11
figure 11

SEM/EDX analysis of AgNW-modified CO and CV fabrics before and after 25 and 50 washes (CO10AgNWs/25 and CO10AgNWs/50) and 1 and 2 washes (CV15AgNWs/1 and CV15AgNWs/2)

Full size image
Table 2 Surface resistance of CO10AgNW and CV15AgNW fabric before and after washing
Full size table

In the SEM/EDX technique, only the surface is analyzed because thermogravimetric analysis as a complementary technique is used. This technique allows for evaluation of the Ag percentage weight over the entire volume of the fabric.

Thermogravimetric analysis

On the basis of the thermogravimetric (TG) analysis, it was noticed that the thermal decomposition of the AgNW colloid started at 392.4 °C with the maximum peak at 430.6 °C. This peak is assigned to polyvinylpyrrolidone (PVP), surrounding and stabilizing the AgNW in colloid. The pattern of PVP powder was also examined, and the thermal decomposition occurred at 414.3 °C with the maximum peak at 434.0 °C (Table 3; Fig. 12). Based on the weight loss value of PVP and AgNW colloid, the amount of AgNWs in the colloid was 37.84%. The concentration of silver nanowires in ink was studied by Tao et al. (2013). They prepared ink with 15% solid content. Based on TG/DTG analysis, they confirmed that the ink contained 15.2% silver nanowires.

Table 3 TG/DTG data of PVP, AgNW colloid, unmodified and modified cotton and viscose fabrics
Full size table
Fig. 12
figure 12

TG/DTG thermogram of PVP and AgNW colloid

Full size image

The peaks near 414 °C (CO10AgNWs) and 385 °C (CV15AgNWs) came from PVP (Table 3; Fig. 13). The amounts of AgNWs for CO1AgNW and CO10AgNW fabric were 1.15 and 13.77%, respectively (Table 3; Fig. 10). For CO10AgNW fabric after 25 and 50 washes, the amount of AgNWs decreased slighty to 10.62% (CO10AgNWs/25) and 10.75% (CO10AgNWs/50), respectively (Table 3). The amounts of AgNWs after 1, 10 and 15 dippings of the CV fabric were 1.89, 9.97 and 14.12%, respectively (Table 3; Fig. 13). After the first (CV15AgNWs/1) and second (CV15AgNWs/2) washes of CV15AgNW fabric, the amount of AgNWs decreased from 14.12 to 5.71% and 4.47%, respectively (Table 3). It was observed that the effect of AgNW modification of the CV fabric was not resistant to washing as opposed to CO fabric.

Fig. 13
figure 13

TG/DTG thermogram of a AgNW colloid, unmodified and modified cotton fabrics and b AgNW colloid, unmodified and modified viscose fabrics

Full size image

The Ag content of modified fabrics obtained from SEM/EDS and TG analysis is different because of various measurement techniques. As mentioned at the beginning, the sample in TG analysis is measured over the entire volume, while in SEM/EDS analysis only the surface is analyzed. However, despite these differences, the relationship of the Ag content depending on the dipping number is preserved or similar, e.g., for CO1AgNW and CO10AgNW fabrics the Ag content is 1.15 and 13.77%, respectively. From SEM/EDS, the Ag content is 3.8 and 53.2% for CO1AgNW and CO10AgNW fabrics, respectively.

Durability

For the best conductive CO10AgNW and CV15AgNW fabrics, abrasion resistance tests were carried out. No changes in the electrical conductivity of CO10AgNW and CV15AgNW fabrics were observed. After abrasion, the values of R s were 23 ± 3 and 48 ± 3 Ω for CO10AgNWs and CV15AgNWs, respectively. Also, no changes in the AgNW layer on SEM images were observed (not shown). The AgNW coatings were durable, and abrasion did not influence the conductivity of either fabric.

For the AgNW colloid synthesis, PVP was used as an AgNW stabilizer. PVP on AgNW-modified fabrics using FTIR/ATR, Raman and TG analysis was confirmed (Figs. 6, 7, 8, 9, 12, 13). The presence of this stabilizer does not interfere with the interaction between silver nanowires and the conductivity of modified fabrics, although PVP has moderate electrical conductivity 7.42 × 10−8 S cm−1 (Ravi et al. 2013). The presence of PVP is necessary because the surrounding of AgNWs by a thin layer of PVP allows for the separation of each nanowire and creates a conductive network of nanowires on the fabric surface.

The impact of AgNW modification on the mechanical properties of both fabrics was evaluated. The results of the tensile strength test for modified CO10AgNW and CV15AgNW fabrics showed the growth of breaking force about 49% from 241N (CO) to 472N (CO10AgNWs). However, for CV15AgNW fabric the breaking force decreased from 574N to 420N (about 27%). No changes of breaking elongation before and after AgNW modification were noted. The breaking elongation for CO and CO10AgNW fabrics is 10.2 and 9.90%, respectively, and for CV and CV15AgNW fabric is 19.40 and 19.90%, respectively. Similar results of lower strength viscose fabric after modifications (among others with TiO2) were observed in our previous work (Giesz et al. 2016).

The differences in the results of AgNW application, durability of the modification effect and changes of tensile strength for two cellulose fabrics are related to the variety of their morphological and topographical structures, discussed by Giesz et al. (2016).

Antibacterial effect

The Ag content for CO10AgNW and CV15AgNW fabrics is similar, but other properties such as the tensile strength are worse for CV15AgNWs; therefore, the antibacterial properties were evaluated for CO10AgNW fabric against S. aureus and K. pneumoniae bacteria. No reduction in either bacteria colony was found in the case of unmodified CO fabric. The percentage reduction of S. aureus and K. pneumoniae seeded on CO10AgNW fabric was 94.7 and 97.7%, respectively, and we can conclude that such modification of CO fabric is effective against gram-positive and -negative bacteria. The good antibacterial effect could be attributed to a high degree of surface coverage with AgNWs.

Conclusions

Multifunctional cotton and viscose fabrics modified with silver nanowires (AgNWs) by the dipping-drying method were obtained. AgNW loading on the fabric surfaces gives them conductive properties, which depend on the amount of AgNWs and connections between nanowires. To achieve good electrical conductivity, the dipping process in AgNW colloid was repeated 10 times and 15 times for cotton (CO10AgNWs) and viscose (CV15AgNWs) fabrics, respectively. More effective modification of cotton compared to viscose fabric was observed. The average surface resistance of 20 and 46 Ω was Ag 53.2 wt% for CO10AgNW and Ag 52.3 wt% for CV15AgNWs, respectively. The electrical conductivity of CO10AgNWs dropped slightly after 50 washes (R s increased from 20 to 195 Ω), while for CV15AgNWs after two washes, the fabric beceme nonconductive (R s increased from 46 to 1.4 × 1011 Ω). The AgNW layer on the fabric surface is resistant to abrasion. The tensile strength after modifications with AgNW colloid increased about 49% for CO10AgNW fabric and decreased about 27% for CV15AgNWs. The AgNW-modified cotton fabric surface caused a significant antibacterial effect against gram-positive (S. aureus) and -negative bacteria (K. pneumoniae). The effectiveness of the modification depends on the type of cellulose textile material used. The presented modification method with AgNWs is more suitable for cotton than for viscose fabric. Cotton fabric modified with AgNWs preserves its mechanical properties and retains its conductivity even after many washings. The developed electroconductive and antimicrobial cotton fabric can be used in further studies concerning E-textiles.