Statistical Optimization of the Sol–Gel Electrospinning Process Conditions for Preparation of Polyamide 6/66 Nanofiber Bundles
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Polymeric nanofibers are widely studied in the textile industry since with them, it is possible to get a great variety of functionalities. In this paper, polyamide 6/66 (PA 6/66) solutions at different concentrations (12, 17, and 22% wt.) were made, to get nanofibers through the basic electrospinning process which were characterized by scanning electron microscope (SEM) and productivity. Afterwards, nanofiber bundles were produced using the electrospinning sol–gel process, which were characterized by SEM and tensile test. From the results of statistical optimization based on one-way analysis of variance (ANOVA) with post hoc Tukey HSD, it was found that nanofiber bundles with higher productivity (1.39 ± 0.15 mg/min), draw ratio (9.0 ± 1.2), and tensile strength (29.64 ± 7.40 MPa) were obtained with a 17% concentration. Finally, a thermal characterization through differential scanning calorimetry (DSC) was done, finding evidence of a Tg and Tm reduction in the nanofibers in relation to PA 6/66 pellets and nanofiber bundles.
KeywordsSol–gel electrospinning Polyamide 6/66 Nanofiber bundles Scanning electron microscope Differential scanning calorimeter
Differential scanning calorimetry
- PA 6/66
Scanning electron microscope
Nylon is a polymer classified as polyamide that was discovered by Wallace Hume Carothers in 1934; it is produced as fiber and plastic depending on the processing conditions . Commercially, there are different kinds of nylon, nylon 6, nylon 66, nylon 6, 10, etc., having in common the amide functional group (–CO-NH-) . This polymer is used to produce blown films and monofilaments through spinning processes, and it can be copolymerized. Such is the case of nylon 6/66 which is produced to lower melting temperature compared to nylon 6. In the last few years, nylon has been used in multiple applications such as women stockings, parachutes, zippers, fishing lines, bridal veils, carpets, musical strings, and rope .
Conventional filament and nylon thread transformation processes are wet spinning, dry spinning, and gel spinning and allow to manufacture between 20- and 400-μm diameter filaments . These processes, which are carried out from polymeric solutions, are dependent on the concentration, since their variation affects the stretching ratio and consequently the mechanical properties of the fibers .
The electrospinning process  is used, even at a nanometer scale, to get nylon fibers of a smaller diameter . It also allows to make polymeric nanofibers with polarities, porosities, and adjustable diameters that can additionally be adapted to a wide variety of sizes and shapes. Besides, by using this technique, it is possible to control the properties, functionality, and composition of the nanofibers through the polymer concentration and electrospinning parameters . Ramkrisna et al.  affirm that the morphological result of the electrospinning process presents a high concentration dependence, as a similar way with conventional spinning processes ; since a higher concentration leads to a higher viscosity in the polymer solution, for this reason, the study of this article evaluates the concentration of the polymer as unique variable in a unifactorial design. This is important to evaluate the possibility of carried out on an industrial scale.
Polymeric nanofibers obtained through electrospinning can be used in many fields in industry: scaffolds, sensors, filters, membranes, batteries, protective clothing, wound dressing, and catalyst . In the textile area, nanofibers are used to get specific functionalities such as self-cleaning fabrics, virus and bacteria repellent, temperature control, sensors, and filters . Also, some other textile applications have been reported as antibacterial clothing , wound dressings , and protective clothing  thanks to their chemical properties and mechanical strength.
PA 6/66, reference Ultramid C40 L, Basf brand was used. As solvent, a mixture of formic acid and acetic acid was used, and distilled water as the coagulation bath.
Preparation of Polyamide Solutions
Solutions were prepared at different concentrations in weight 12%wt., 17% wt., and 22% wt., using a mixture of formic acid and acetic acid as solvent in a mass relation of 4:1 , at room temperature and continuous stirring.
Basic Electrospinning Process
In all the process carried out with the solutions at different concentrations, a voltage of 27.5 kV was used, supplied by a Gamma High Voltage Research Inc. Model E30 equipment connected to a metal needle placed at 12 cm from the collector. The flow of the solution was controlled by a syringe pump from Braintree Scientific Syringe Pump Brand Inc. which was set between 0.3 and 1 ml/h.
Electrospinning Sol–Gel Process
This process was carried out using a coagulation bath of distilled water and a tensile cylinder’s system with speed control. We got nanofiber bundles of PA 6/66 at three concentrations (12, 17, and 22%), following a unifactorial design completely random with three replicas and a significance level of α = 0.05. Studied variables were productivity in the deposit of nanofibers, draw ratio, and nanofiber bundle tensile strength. It is important to note that concentrations less than 12% by weight were not evaluated, since in preliminary tests this condition did not allow the formation of electrospinning nanofibers; in the same way, no concentrations greater than 22% by weight were evaluated, because the resulting viscosity was very high, hindering agitation in the preparation of the solution and subsequent flow in the electrospinning process. Additionally, only extreme concentrations and the midpoint were investigated.
For the basic electrospinning process, for each concentration, the productivity (mg/min) in the deposit of electrospun nanofiber mats of PA 6/66 was determined. Afterwards, these were morphologically characterized through scanning electron microscope (SEM).
For the electrospinning sol–gel process, after adjusting process variables (voltage, flow, needle–collector distance), to get a stable and continuous electrospun jet, the draw ratio of the process was determined, then the obtained PA 6/66 nanofiber bundles were characterized through SEM and tensile test. Finally, the process optimal condition was characterized through differential scanning calorimetry (DSC).
The samples were coated in gold in a vacuum coating machine [Denton Vacuum Desk IV] for about 200 s. At the end, they were deposited in the sample holder of scanning electron microscope (JEOL JSM 6490 LV, Japan), equipped with tungsten filament. Afterwards, we induced a 30 Pa vacuum in the chamber to generate electrons, to scan and to get images. Then, with the image software, average nanofiber diameters were measured.
Three hundred threads of nanofiber bundles were tested with a testing machine (EZ-Test L, Shimadzu, Japan) at a trial speed of 30 mm/min and a reference length of 50 mm according to the ASTM D3822 standards.
To determine phase transitions, the differential scanning calorimetry (DSC) technique was used following ASTM D3418-08 standard applied to the polymeric material analysis. We employed a differential scanning calorimeter (DSC) (TA Instruments, Q20, USA) with 5-mg samples that were deposited in hermetically sealed aluminum crucibles and subjected to two consecutive heating cycles from 25 to 250 °C at a 10 °C/min speed with 5 min isotherms between each cycle. The TA Universal Analyzer® Software, adapted to the equipment, allowed to get the thermograms in order to determine the glass-transition temperatures and material fusion.
Results and Discussion
Productivity of the Basic Electrospinning Process
Morphology/Morphological Characterization of PA 6/66 Nanofibers
Draw Ratio in the Electrospinning Sol–Gel Process
PA 6/66 Nanofiber Bundle Morphology/Morphological Characterization
Nanofiber Bundle Tensile Strength
Additionally, the average result of tensile strength obtained with the 17% nylon (29.64 MPa) concentration was similar to the one reported by Wu et al.  in their research presenting results of 66 polyamide nanofibers firstly electrospun and then bent with strength values near 30 MPa.
Optimal Process Condition
DSC Thermal Analysis of the Optimal Condition Nanofiber Bundles
Thermal parameters obtained by DSC results
Nanofiber bundles 17%
It may be observed from the Tg results that nanofibers at a 17% concentration show a higher intermolecular mobility, compared to the nanofiber bundles at the same concentration. The latter is explained because the increased molecular mobility is caused by a rise in the polymer chain space called free volume, which reduces interactions among them. This way, chains with greater mobility require lower temperature for the transition from vitreous solid to rubbery, resulting in lower Tg values.
The melting temperature value is associated with the required temperature to melt the ordered structures (crystals) into the polymer, and its variation is related to the crystal size. It may be noted that nanofibers at a 17% concentration showed the lowest value in the melting temperature compared with the PA and nanofiber bundles at the same concentration. This indicates that the basic electrospinning process and electrospinning sol–gel reduced the amount of crystalline regions of the polymer in relation to the pellets, turning them into fibril structures , which through the spinning and the applied draw ratio, oriented the polymeric chains and showed a recovery in the crystallinity degree of the nanofiber bundles in a 44.71% compared to nanofibers. Finally, the enthalpy of fusion reveals the crystallinity amount in the analyzed polymer , and its value is associated with the required energy in the crystalline structure fusion. This proves that nanofibers at a 17% concentration demand less energy to melt than the crystalline structures from the nanofiber bundles and the PA 6/66 pellets.
6/66 polyamide electrospinning sol–gel process showed a significant increase in the productivity (1.39 ± 0.15 mg/min), draw ratio (9.0 ± 1.2), and tensile strength (29.64 ± 7.40 MPa) for a 17% concentration in weight compared to the other two tested concentrations (12% wt. and 22% wt.). This statistically optimized process condition allowed us to get uniform PA 6/66 nanofiber bundles from a stable and continuous process.
Thanks to University of San Buenaventura, Cali, for all the support through the Research Project: “Development of a Composite Material Based on Thermoplastic Starch Strengthened with Polymeric Nanofibers for Its Use as Leather in Costume Design.”
This study was supported financially by the University of San Buenaventura, Cali, Colombia (34606025).
Availability of Data and Materials
The datasets used for analysis can be provided on a suitable request, by the corresponding author.
EF proposed the research work and wrote the paper. MA carried out the statistical design of experiment. RD and DN prepared the SEM and DSC. All authors helped to correct and polish the manuscript and read and approved the final manuscript.
The authors declare that they have no competing interests.
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
- 1.Ebewele RO (2000) Polymer science and technology. Polym Sci Technol 483. https://doi.org/10.1016/0025-5416(85)90434-3
- 4.Gupta VB, Kothari VK (1997) Manufactured fibre technology. Springer Netherlands. https://www.springer.com/us/book/9780412540301
- 5.Nakajima T, Kajiwara K, McIntyre JE (1994) Advanced fiber spinning technology. Woodhead. https://www.sciencedirect.com/science/book/9781855731820
- 6.Uslu İ, Altaş A, Aksu ML, Gökmeşe F (2009) Nanofibers by electrospinning of nylon 6 doped with boron. Academia.Edu 37:55–60Google Scholar
- 7.Agarwal S, Jiang S (2015) Nanofibers and electrospinning. In: Encyclopedia of polymeric nanomaterials. Springer Berlin Heidelberg, Berlin, Heidelberg, pp 1–15Google Scholar
- 9.Ramakrishna S (2005) An introduction to electrospinning and nanofibers. World Scientific. https://www.worldscientific.com/worldscibooks/10.1142/5894
- 11.Ebara M, Kotsuchibashi Y, Uto K et al (2014) Smart nanofibers. Springer, Tokyo, pp 189–235Google Scholar
- 15.Franco E (2015) Electrohilado de nanofibras de polivinil alcohol Refuerzo secundario de pastas de cemento portland ultrafino. Publicia. https://www.morebooks.de/store/es/book/electrohilado-de-nanofibras-de-polivinil-alcohol/isbn/978-3-639-64950-5
- 19.Gupta RK (2000) Polymer and composite rheology. Marcel Dekker. https://books.google.com.ar/books?hl=es&lr=&id=0UZZDwAAQBAJ&oi=fnd&pg=PP1&dq=Gupta+RK+(2000)+Polymer+and+composite+rheology.+Marcel+Dekker&ots=4u38V7umfp&sig=kPcAPw9b0ZApyuUILodXQKzPbAI#v=onepage&q=Gupta%20RK%20(2000)%20Polymer%20and%20composite%20rheology.%20Marcel%20Dekker&f=false
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