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Article

Fluid Flow in Cotton Textile: Effects of Wollastonite Nanosuspension and Aspergillus Niger Fungus

by
Ayoub Esmailpour
1,
Hamid R. Taghiyari
2,*,
Reza Majidi Najafabadi
3,
Amin Kalantari
2 and
Antonios N. Papadopoulos
4,*
1
Department of Physics, Faculty of Sciences, Shahid Rajaee Teacher Training University, Tehran 16788-15811, Iran
2
Wood Science and Technology Department, Faculty of Materials Engineering & New Technologies, Shahid Rajaee Teacher Training University, Tehran 16788-15811, Iran
3
Department of Restoration, Central Tehran Branch (IAU–CTB), Islamic Azad University, Poonak Sq., Ashrafi Esfehani Ave., Tehran 15847-43311, Iran
4
Department of Forestry and Natural Environment, International Hellenic University, GR-661 00 Drama, Greece
*
Authors to whom correspondence should be addressed.
Submission received: 2 November 2019 / Revised: 26 November 2019 / Accepted: 27 November 2019 / Published: 2 December 2019
(This article belongs to the Section Materials Processes)

Abstract

:
Aspergillus niger is a common contaminant in food industry, laboratories, and also a potential threat to biological works of art in museums. Cotton textiles have frequently been used in museums for canvas paintings. In the present project, the effect of Aspergillus niger on fluid flow rate of nanowollastonite-impregnated cotton textile specimens was investigated. Cotton specimens were impregnated with nanowollastonite (NW) suspension at four concentrations of 10%, 20%, 30%, and 40% to be further compared with control specimens. Results showed that fluid flow in cotton textile was as high as 361.3 cm3·s−1 due to its high porous structure and very low compactness of fibers (low density). Impregnation with NW did not have a significant effect on fluid flow in cotton textile. Exposure to Aspergillus niger increased fluid flow in control specimens as a result of deterioration of cotton fibers. Exposure of NW-impregnated specimens at concentrations more than 20% to Aspergillus niger did not have any significant effect on fluid flow. In control specimens, fungus mycelium penetrated deep into the texture of textile. However, in NW-impregnated specimens, the fungus could not penetrate into the texture and deteriorate the specimens. It was concluded that NW can be recommended for textile industry and also works of art as they protect cotton textiles against Aspergillus niger while, do not diminishi its dying and paintability properties.

1. Introduction

Fungi spores can move easily even by air movement, landing on precious materials such as papers and textiles in museums. Exposure of historical objects in museums to fungi is inevitable. Textiles made from ligno-cellulose and biomaterials can therefore be degraded by different deteriorating agents such as fungi [1,2,3,4,5]. Cotton textiles are basically cellulose fibers woven together; this makes them vulnerable to a variety of fungi species, including Aspergillus, Penicillium, Chaetomium, Trichoderms, and Alternaria species [3]. The genus Aspergillus has many species, including Aspergillus niger. As a common fungus species, it is a troublesome fungus that causes a disease called black mold, is contaminant of different edible materials (such as fruits and vegetables), and it grows on cellulosic materials too. The easy access of this fungus to artistic objects in museums makes them at constant risk of being destroyed. Many fungicide and polymers and nanomaterials have so far been experimented to increase biological resistance of textiles and fabrics in museums [3]. Abdel-Kareem [4] used four polymers mixed with different fungicides. Some dominant fungi isolated from ancient Egyptian textiles were used to be tested on sample textiles. The cited author reported increased durability and reinforcement of the textiles. Though, improvement was observed in the abovementioned research projects, application of chemicals and polymers as fungicides are to be limited in favor of more environmentally friendly materials. Wollastonite is mineral material, having no environmental contamination and being safe regarding human health; moreover, its application on historical objects would have no harm on the objects themselves [6,7,8]. It has shown high efficacy to limit fungi growth on lingo-cellulosic materials such as cotton textiles and papers by simple spraying or dipping in a wollastonite suspension, and wood and wood-composites by impregnation and mixing with resins [9,10,11]. Therefore, in the present project, wollastonite was used to find out if it can have hindering effects on the growth of fungi on cotton textiles which are constantly used in paintings of museums. In order to increase effectiveness of wollastonite and to benefit from the advantages of materials at nanoscale [12,13,14,15,16], wollastonite nanosuspension with four concentrations were used to impregnate cotton textile specimens. Specimens were then exposed to Aspergillus niger [17], as a dominant fungus species in Moghadam Museum of University of Tehran. This fungus was extracted and identified from historic embroidery at the abovementioned museum (Figure 1). This embroidery contains colored silk textile pieces that are sewn on a cotton substrate (Figure 2). Colored silk threads were used to create shapes on silk textiles, and also to sew silk textile pieces and cotton substrate together (Figure 3).
Though previous studies have already illustrated the effectiveness of nano-wollastonite (NW) in preserving ligno-cellulose materials, including some textiles that are used in museums [9,10,17,18], further studies should be done to investigate other properties of currently used textiles as to the importance of artistic objects in museums. Therefore, the present project was carried out to elaborate on permeability, as an important physical property that ultimately affects dying and printability in textiles.

2. Materials and Methods

2.1. Specimen Preparation and Nano-Wollastonite Impregnation

White cotton textile with no dye was purchased from Tehran Central Bazaar. Specimens were prepared with dimensions of 40 × 40 mm (Figure 4). Specimens were randomly divided into six groups. Four sets of specimens were impregnated with nano-wollastonite suspension (NW) with 10%, 20%, 30%, and 40% concentrations. For preparation of NW-suspension with the target concentration for example 20%, 20 g of nano-wollastonite gel (based on the dried weight) was mixed with an appropriate amount of distilled water (in this case, 80 g distilled water). The mixture was then mixed for 20 min by a magnetic stirrer. Once NW-suspensions with the target concentration were prepared, cotton specimens were dipped in them for 30 s, during which they were gently shaken steadily. After being impregnated, each specimen was separately hung up to dry (25 ± 2 °C; relative humidity 40%–43%). The results of permeability measurement of different NW-treated specimens were finally compared with those of the control specimens (without NW impregnation). For each group, 20 specimens were prepared; in total, 100 specimens were tested in the present study.
At least 70% of wollastonite nanofibers ranged from 30 to 110 nm. Specifications of wollastonite compounds and formulations were as presented in Table S1 (Supplementary Material No. 1). Once impregnated, specimens were hung to season for 6 weeks before being exposed to Aspergillus niger fungus. The control specimens were exposed to the fungus under the same conditions. Before and after the impregnation, fluid flow in all specimens was measured for comparison purposes.

2.2. Volumetric Flow Rate Measurement

Flow rate was measured by an apparatus to measure air permeability in continuous porous media [19]. The volume displacement of falling-water was measured to determine volumetric flow rate [20]. Milli-second precision was used to measure the volume of the falling-water. The 40 × 40 mm specimens were put in a special holder for measurement of the air flow rate; diameter of the flow area of paper specimens were set according to air resistance of paper, Gurley method (Figure 5). The whole system was airtight. Pressure difference (∆P) was monitored in milli-bar precision [20]. An electronic time measurement device was connected to the apparatus to determine the time with milli-second precision. As the volume in the water tube could easily be measured, the volumetric flow rate was calculated in terms of cm3 s−1.

2.3. Fungal Exposure

In the present study, cotton textile specimens were first dried at 103 ± 2 °C for 24 h in a hot air oven. The weight of each specimens was measured before and after fungal exposure. Once dried, they were exposed to A. niger for 3 months in Petri dishes. Petri dishes were inoculated 3 weeks before cotton specimens were placed in them to be exposed to A. niger. In order to make sure all specimens were exposed to the same density of A. niger, only those Petri dishes were selected in which A. niger mycelia covered 70%–80% of the substrate nourishing substance.
The incubation process was performed at the National Library and Archives of I. R. of Iran on Sabouraud’s agar (25 ± 1 °C and 45% ± 2% relative humidity). Mycelia that were grown on the specimens were then carefully removed and specimens were dried again before the final fluid flow measurement.

3. Results and Discussion

Results of the flow rate measurement demonstrated that the permeability in cotton textile was high compared to other cellulosic materials such as paper, wood, and wood-composites; flow rate in the control specimens of cotton textile was 361.3 cm3·s−1 (Figure 6). A previous study reported that fluid flow rate in historical paper was as low as 29 cm3·s−1. Density of the cotton textile in the present project was 0.51 g·cm−3, while the density of the historical paper was 1.15 g·cm−3. This indicated that compactness ratio in the historical paper was significantly higher in comparison to the cotton textile. Therefore, fluid could more easily pass through the voids and spaces in between the fibers in cotton textile. In fact, the higher density in the historical paper can be translated into a more integrated matrix, and lower voids and spaces in between the fibers, ultimately hindering any fluids to pass through. Cross-sectional macrophotos of control specimens showed large cavities in between fibers, allowing fluid to easily pass through (Figure 7).
NW-impregnation did not have any significant effect on flow rate (Figure 6). Considering the significant effect of NW-impregnation on historical paper, and bearing in mind its higher density and compaction ratio, this may indicate that the porous structure in cotton textile specimens was so wide that the formation of new bonds between Calcium atoms in wollastonite and oxygen atoms in the hydroxyl groups of the cellulose chains could not alter its fluid flow behavior [21,22]. In this connection, density functional theory (DFT) previously illustrated that the optimal adsorption distance and adsorption energy for NW on cellulose were 1.7 Å and −6.6 eV, respectively [22], that are considerably high.
Once exposed to Aspergillus niger, only the control and NW-10% specimens showed an increase in fluid flow rate (7.5% and 8.5% in the control and NW-10%, respectively). The increase was attributed to the deteriorating effect of Aspergillus niger on textile fibers, decreasing their integrity and eventually, allowing a larger volume of air to pass through. The same deteriorating effect was reported to have caused considerable decline in tensile stress of cotton textile [18]. The similar increase in fluid flow rate in the control and NW-10% specimens indicated that 10% of NW is not enough to significantly hinder the growth of A. niger on cotton textile. On the other hand, higher NW concentrations (NW-20%, NW-30%, and NW-40%) demonstrated a decrease in flow rates (Figure 6). A previous research project demonstrated that NW concentration of 20% significantly improved the biological resistance of cotton textile in a way that tensile stress values in the fungal-exposed NW-impregnated specimens were significantly similar to those of the control specimens [18]. Based on the above discussion, it was concluded that higher NW concentrations preserved the overall structure of cotton textile in a way that fungi mycelium could not penetrate deeply into textile structure and deteriorate it; instead the mycelium had to spread on the outer layer of textile specimens. Microscopic images of the surface of cotton specimens showed A. niger mycelium to fully grow and fill in the voids and empty spaces among the cotton fibers, regardless of being impregnated with NW or not (Figure 8a–c). However, the cross-sectional view of specimens demonstrated that in control and NW-10% specimens, Aspergillus niger mycelium penetrated into deep parts of the textile profile cut (Figure 9a). However, in specimens impregnated with higher NW concentrations, mycelium had a tendency to accumulate only on the surface layers (Figure 9b).
The r-square value of 66% between fluid flow values versus tensile stress indicated that although fluid flow in cotton textile as a porous media was closely in relation with the integrity of the overall matrix, other elements were also involved in the process (Figure 10). In this connection, considering highly significant decreasing effect of fungal exposure on tensile stress and tensile strain values in a previous study [18], higher increase in fluid flow was expected. However, it is to be noted that growth of thick mycelium network on and within voids and spaces of control specimens partially blocked the way through transfer of fluid (Figure 9a). In fact, an increase in weight was reported in specimens as a result of being exposed to Aspergillus niger [18]. Therefore, fluid flow rate could not increase higher. In the NW-40% specimens though, Aspergillus niger could not easily grow into the texture and the growth was rather superficial (Figure 9b). Contour and surface plots clearly showed a steady decreasing trend in fluid flow as tensile strain and tensile stress values decreased (Figure 11).
Cluster analysis based on the properties of fluid flow, and tensile stress and strain values clearly revealed that exposure to Aspergillus niger fungus had a nearly similar effect on the control and NW-10% specimens (Figure 12). This similarity was also observed in the fluid flow values of these two treatments (Figure 6). Therefore, it is concluded that NW suspension with 10% of concentration would not be sufficient to significantly improve biological resistance of cotton textile against Aspergillus niger fungus. Other treatments demonstrated close cluster-grouping, indicating an overall similarity among them. Therefore, nearly any of the 20%, 30%, or 40% NW-concentrations can be recommended.

4. Conclusions

The aim of this study was to investigate the effects of Aspergillus niger on fluid flow of cotton textiles impregnated with four concentrations of nanowollastonite. Exposure to Aspergillus niger increased fluid flow rate in control specimens as a result of deterioration of fibers in cotton specimens and it was found that fungus mycelium can penetrate deep into the texture of textile. In nanowollastonite impregnated specimens, the growth of Aspergillus niger occurred mainly on the superficial layers of cotton textile and fluid flow rate with concentrations higher than 20%, remained rather intact with a slight tendency to decrease in value. It is concluded that impregnation with nanowollastonite suspensions can be recommended for textile industry and for canvas paintings because it does not change fluid flow as a vital criterion in textile determining dying and paintability of textiles and fabrics, while protecting these materials against deterioration by Aspergillus niger. However, as impregnation can affect surface roughness and, therefore, dying and paintability of textiles and fabrics would change, further studies on surface roughness and paintability should be undertaken to conclude on this point.

Supplementary Materials

The following are available online at https://0-www-mdpi-com.brum.beds.ac.uk/2227-9717/7/12/901/s1, Table S1: Compounds of the nano-wollastonite gel used for treatment purpose at four concentration levels of 10, 20, 30, and 40%.

Author Contributions

Methodology, H.R.T., A.E. and R.M.N.; Validation, H.R.T. and R.M.N.; Investigation, R.M.N. and A.K.; Writing-Original Draft Preparation, H.R.T., A.E. and A.N.P.; Writing-Review & Editing, H.R.T., and A.N.P.; Visualization, H.R.T. and R.M.N; Supervision, H.R.T.

Funding

This research received no external funding.

Acknowledgments

We appreciate Olaf Schmidt (Dept. of Wood Biology, University of Hamburg) for his valuable scientific consultation and support, as well as Alexander von Humbolt Stiftung, Germany.

Conflicts of Interest

The authors declare no conflict of interest.

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Figure 1. Front view of the historic embroidery at Moghadam museum (Tehran) contaminated with Aspergillus niger fungus.
Figure 1. Front view of the historic embroidery at Moghadam museum (Tehran) contaminated with Aspergillus niger fungus.
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Figure 2. Back view of the historic embroidery at Moghadam museum (Tehran) showing the cotton substrate on which silk textile pieces were sewn.
Figure 2. Back view of the historic embroidery at Moghadam museum (Tehran) showing the cotton substrate on which silk textile pieces were sewn.
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Figure 3. Shapes created by silk threads stitches on the historic embroidery at Moghadam museum (Tehran).
Figure 3. Shapes created by silk threads stitches on the historic embroidery at Moghadam museum (Tehran).
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Figure 4. Photograph of fluid flow samples with dimensions of 40 × 40 mm.
Figure 4. Photograph of fluid flow samples with dimensions of 40 × 40 mm.
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Figure 5. Paper holder for flow rate measurement in paper specimens.
Figure 5. Paper holder for flow rate measurement in paper specimens.
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Figure 6. Volumetric flow rate (cm3·s−1) in the textile specimens before and after being impregnated with wollastonite nanosuspension and after being exposed to A. niger fungus (NW = nanowollastonite; F = fungus-exposed) (letters on each column represent Duncan groupings at 95% level of confidence).
Figure 6. Volumetric flow rate (cm3·s−1) in the textile specimens before and after being impregnated with wollastonite nanosuspension and after being exposed to A. niger fungus (NW = nanowollastonite; F = fungus-exposed) (letters on each column represent Duncan groupings at 95% level of confidence).
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Figure 7. Cross-sectional of control textile specimen showing large cavities in between fibers for transfer of fluid.
Figure 7. Cross-sectional of control textile specimen showing large cavities in between fibers for transfer of fluid.
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Figure 8. Surface views of a control with no fungal exposure (a), as well as control (b) and NW-40% (c) specimens after being exposed to A. niger.
Figure 8. Surface views of a control with no fungal exposure (a), as well as control (b) and NW-40% (c) specimens after being exposed to A. niger.
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Figure 9. Cross-sectional of fungus-cultured specimens showing penetration of A. niger mycelium in deeper parts of control specimens (a), and accumulation of mycelium in the surface layers of NW-40% (b).
Figure 9. Cross-sectional of fungus-cultured specimens showing penetration of A. niger mycelium in deeper parts of control specimens (a), and accumulation of mycelium in the surface layers of NW-40% (b).
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Figure 10. Fitted-line plot between fluid flow versus tensile stress values.
Figure 10. Fitted-line plot between fluid flow versus tensile stress values.
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Figure 11. Contour and surface plots among tensile stress and tensile strain versus fluid flow values (Ten-Stress = tensile stress; Ten-Strain = tensile strain).
Figure 11. Contour and surface plots among tensile stress and tensile strain versus fluid flow values (Ten-Stress = tensile stress; Ten-Strain = tensile strain).
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Figure 12. Cluster analysis of the control and NW-impregnated cotton textile specimens based on tensile stress and strain, as well as fluid flow, values before and after exposure to A. niger fungus for 3 months (F = fungal-exposed; NW = nano-wollastonite).
Figure 12. Cluster analysis of the control and NW-impregnated cotton textile specimens based on tensile stress and strain, as well as fluid flow, values before and after exposure to A. niger fungus for 3 months (F = fungal-exposed; NW = nano-wollastonite).
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MDPI and ACS Style

Esmailpour, A.; Taghiyari, H.R.; Najafabadi, R.M.; Kalantari, A.; Papadopoulos, A.N. Fluid Flow in Cotton Textile: Effects of Wollastonite Nanosuspension and Aspergillus Niger Fungus. Processes 2019, 7, 901. https://0-doi-org.brum.beds.ac.uk/10.3390/pr7120901

AMA Style

Esmailpour A, Taghiyari HR, Najafabadi RM, Kalantari A, Papadopoulos AN. Fluid Flow in Cotton Textile: Effects of Wollastonite Nanosuspension and Aspergillus Niger Fungus. Processes. 2019; 7(12):901. https://0-doi-org.brum.beds.ac.uk/10.3390/pr7120901

Chicago/Turabian Style

Esmailpour, Ayoub, Hamid R. Taghiyari, Reza Majidi Najafabadi, Amin Kalantari, and Antonios N. Papadopoulos. 2019. "Fluid Flow in Cotton Textile: Effects of Wollastonite Nanosuspension and Aspergillus Niger Fungus" Processes 7, no. 12: 901. https://0-doi-org.brum.beds.ac.uk/10.3390/pr7120901

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