1,2Department of Mechanical Engineering, JNTUH University College of Engineering, Hyderabad, Telangana, 500085, India
3
Department of Mathematics, JNTUH University College of Engineering, Hyderabad, Telangana, 500085, India
Corresponding author details:
Kumar KS
Department of Mechanical Engineering
JNTUH University College of Engineering
Telangana, 500085,India
Copyright:
In the present paper, Nylon is taken as the matrix material, and composite is
made by the addition of the MgO at various percentages based upon Taguchi’s design
of the experiment, After fabrication of the composite material, the tensile and wear
test is carried out to see the variation of the mechanical properties, and optimum
process parameters are found using the Anova test and along with varying the
process parameters such as normal load, sliding distance, and speed. The surface of
the material after braking is studied using SEM Analysis and also the wear debris is
studied, and results were obtained as there is an impact of MgO on the matrix material.
Nylon-6, MgO; Tensile; Wear test; Taguchi; Scanning Electron Microscope
Teflon as a filler to Nylon 6 matrix material increases the tensile and the hardness
of the Nylon/Teflon polymer matrix composites. The addition of Teflon to the Nylon
6 matrix increases hardness and tensile strength while it decreases the ductility of
the Nylon/Teflon polymer composites [1]. The composites enhance the mechanical
properties by addition of the filler content, by addition of the 10 wt % of Al2
O3
in the
PA6 matrix exhibited the best performance in flexural strength, tensile strength, and
also shows the best performance in hardness and impact strength [2]. The addition of
the graphite filler into PA6 reduces the wear. The minimum wear loss was found at the
filler content of 25 %wt fractions and the increase in the filler content by up to 25%wt
with a decrease in the coefficient of friction [3]. Nano TiO2 with Nylon-6 shows better
mechanical properties compared to micro ones [4]. With the addition of iron oxide
nanomaterial to Nylon 6/Teflon, the tensile and hardness were doubled [5]. With the
addition of graphite content in the composite, there was a reduction in the strength
with an increase in hardness and also Strength of the PTFE increases and stiffness [6].
Impact strength increases gradually with the increase in micro alumina wt. % up to 6
wt. % and after reduces [7]. Inorganic fillers, such as mica, when added to the polymer
composite, increase the heat resistance, rigidity, and dimension stability [8]. Nylon 6/
graphite powder composites increase thermal stability by adding 0-15 wt % of graphite
[9]. The highest tensile strength was achieved by nano-Al2O3 content in the matrix
material [10]. An increase in nano-SiO2 content improves mechanical properties more
compared to the Nylon-6/ABS blend [11]. The hardness of nylon composites varies by
reinforcement material such as fly ash [12]. Copper nanoparticles in nylon 6 improve
mechanical properties with an increase in the concentration of the copper content [13].
This review says nylon 6 is one of the best polymers for composite matrix. Fillers affect
the composite’s mechanical characteristics. Despite polyamide research, Graphite has
a lesser affinity for PA6. More study is needed to improve graphite’s PA6 affinity [14].
According to Taguchi’s design of experiment, the wear conduct of Nylon-6 loaded
with nanometer-measured boron nitride (BN) composites was studied for varying
filler quantity, normal load, sliding distance, and speed. We studied nylon-6 and its
composites using a tensile test. The Nylon-6/BN polymer composites were evaluated
using a pin-on-disk erosion and wear test (ASTM G99). This work reduces extreme
quality in composites by using expanding boron nitride and converts normal load to
a 71.54 percent wear rate variation. Improving Nylon-6/BN composites’ mechanical
characteristics will boost Nylon-6’s use [15]. Load contributes more (81.7%) than
any other input. ABS with 8% MgO has the highest tensile strength. Without MgO,
composites have limited tensile strength. MgO adds mechanical characteristics. MgO enhances composite hardness. Input load increases the wear
rate. ABS/MgO fractography shows that when MgO increases,
multilayer cracks appear due to MgO’sstrong bond with ABS.
According to SEM images, micro fractures increased under load [16].
For improving the wear resistance, the constituent material
MgO with a particle size of approximately 80 nm is taken along
with the matrix material Nylon-6 thermoplastic powder. The
constituent material magnesium oxide is added to matrix
material in various percentages such as 4%, 8%, 12%, 16%, and
20% by weight. To maintain homogeneity, MgO nanoparticles are
mixed in a ME100LA mixer with Nylon-6 thermoplastic powder
at a Temperature of 190°C. The mixing is carried out for 20 min,
maintaining the 200rpm speed of the mixing blades. To fabricate,
the Nylon-6/MgO polymer composites specimens in the injection
molding machine were employed. In a hopper, the mixture
of Nylon-6 and MgO was placed. To make the mixture soft and
smooth the mixture was heated in the barrel. To remove material
shrinkage the blend of liquid Nylon-6 and MgO nanoparticles was
then forced under pressure for a particular time inside a mold
cavity with a constant injection pressure of 70 Mpa. The melt
flow index of Nylon-6 was 12 g per 10 min. And it is a melting
point of the MgO utilized was 230 °
C. For all experiments, the
heating temperature of the charging barrel, injection pressure,
and the cooling time of moldings were kept consistent. The initial
temperature of the mold was 25 °
C. Below the glass transition
temperature, (105 °
C) of the MgO material would solidify. After
an adequate time, the material was solidified into the mold shape
and got ejected. Standard tensile specimens were fabricated
under different injection pressures and packing pressures. A
standard tensile test model was manufactured under various
injection pressures and packing pressures. The specimens used
for the tensile test was shown in (Figure-1). The instrument used
to test the tensile test of the specimen was Tensometer Model PC2000 (Figure 2). This test specimen was investigated by scanning
electron microscope (S-3000N Toshiba SEM) to study the tensile
specimen fracture surfaces at room temperature. conducted for Nylon-6/MgO polymer composites and results
were drawn using Scanning electron microscopy analyses and
found a consequence of wear test of Nylon-6/MgO polymer
composite specimens.
FIGURE1: The spcimens used for the tensile test
Figure 2: Tensometer
Table 1: Design factors with different levels
Table 2: Orthogonal array (L9) and control parameters
Wear and tensile tests for the specimens with varied compositions (4%, 8%, 12%, 16%, 20%wt MgO) were conducted.
Mechanical behaviour of N/MgO polymer composites
Figure 3 describes the stress-strain curves for various compositions of Nylon 6/MgO. Maximum stress is exhibited by 8%wt MgO, and the maximum strain rate is exhibited by 4%wt MgO when compared to other combinations of N/MgO composites. From figure 4(a), it is observed that the ultimate strength increases drastically from 4%wt to 8%wt MgO where the highest ultimate strength is exhibited at 8%wt of MgO (32.74 MPa). From 8% to 16%, tensile strength follows the trend of gradual decrease which resulted in the lowest ultimate strength at 16%wt of MgO (20.52 MPa). It is seen the ultimate strength increases slightly from 16%to 20%wt MgO. The ultimate strength of 4%wt MgO composite and 20%wt MgO are almost the same. From figure 4(b), it can be illustrated that the strain rate observes a drastic decrease from 4%wt to 8%wt MgO. The maximum strain rate is observed at 4%wt MgO. The strain rate increases from 8%wt to 12%wt followed by a gradual decrease trend from 12%wt to 20%wt where it attains the minimum value.
Figure 5 Rockwell Hardness of Nylon 6/MgO polymer composites with different compositions were studied. The hardness of Nylon 6/MgO composites at different compositions follows a linear trend with only a slight difference between each other. Hardness is maximum at 20%wt MgO with a value of 82.16 HRM and a minimum at 8%wt MgO with a value of 74.33 HRM. The hardness decreases slightly from 4%wt to 8%wt, later increases from 8%wt to 12%wt followed by a slight decrease from 12%wt to 16%wt, and finally increases from 16%wt to 20%wt to attain the maximum.
From the table, it was found that the MgO shows a higher contribution. The percentage contribution of the MgO is 75.09% .so; the filler material shows a greater impact on mechanical properties. The second most influencing process parameter is the sliding distance with a percentage contribution of 14.29% - other process parameters such as the speed and the load show very less impact on the output response. The optimum solution was found -12%, load-10 N, speed-300 RPM, and sliding distance-750M.
Development of the mathematical models
Using Minitab, mathematical models are developed to measure the wear rate of the material using input parameters such as filler content, normal load, sliding distance, and speed. The regression equation was developed using the stepwise regression method. The equation is in the form of a coded value. ANOVA test is conducted to know the reliability of the equation and found R2 as 96.03% and R2 (adj) as89.42%. As R2 values are greater than 95% percentage we can adopt the equation for estimating the wear rate.
Confirmation test
To test the regression equation experiment was conducted and wear rates are recorded. The same input values are taken and wear rate was found using the developed equation, and the error percentage compared was found that the error percentage is 7.01 %. The test was conducted by taking input values as MgO -12%, load-20 N, speed-100 rpm, and sliding distance-750 M.
The wear rate was found that 175 µm and the predicted value is 162.7. There is little variation in the experimental values and the predicted values so the equation can be adopted
Fantagraphics of Nylon-6/MgO and nylon 6 polymer composites are shown in figure 6. For pure Nylon-6 there are Voids and fibrillation which were formed due to the debonding in the Nylon-6. Figures 6(b), 6(c), 6(d), 6(e) an 6(f) Nylon-6/MgO polymer composites are shown; there are micro damages. These micro-damages were found until the interface degradation was reached. MgO nanoparticles have been observed on the damaged surface. When a material is broken it was observed that there is a little breakdown of the MgO particles. Rougher surfaces and more crack branching for Nylon-6/4%MgO, Nylon-6/8%MgO, and Nylon-6/20%MgO composites
For trials conditions 1, 2, and 3 with 4% MgO nanoparticles, there are small grooves of worn surfaces appearing as shown in figures 7-9. Deformation and cracking were observed on the surface in Figures 10b and 10c due to the increase in the load and sliding distance. Figure 11c, the situation was difficult for 20 N normal load and 1000 m sliding distance. For trials 4, 5, and 6 with 12% MgO nanoparticles, the high strain experienced by the specimens result in worn surfaces. As the load was increasing worm surfaces were higher. For trials 7, 8, and 9 with 20% MgO nanoparticles, the worn surface is less as compared to trial 9. Large plastic deformation was found for trail 9.
Wear debris was found during the wear tests given in figures 11-12. When load and sliding distance is increased, there is an increase in the size of the platelets or flakes. When the volume fraction of MgO at lower loads there is also found an increase in the flakes.
Figure 3 Ultimate strength (a) and corresponding strain (b)
as a function of MgO.
Figure 4 ; Stress-strain curves of N/MgO polymer composites.
Figure 5: Hardness is a function of %wt MgO
From the table, it was found that the MgO shows a higher
contribution
Figure 6: Fractography of Pure Nylon-6 and Nylon-6/MgO
polymer composites
Table 4: WEAR/µm=1523 - 873 A - 50.3 C - 510 D + 242.0 A2
+ 122.0 D2
Figure 7: Worn surfaces of specimens for trial conditionsof 1, 2, and 3.