Unfilled Natural Rubber Compounds Containing Bio-Oil Cured with Different Curing Systems: A Comparative Study

This study focuses on the properties of unfilled natural rubber compounds containing bio-oils cured with a peroxide curing system and then discusses the comparisons to those cured using the sulfur system from our previous work. Two types of bio-oils, i.e., palm oil and soybean oil, were used, and distillate aromatic extract (DAE)-based petroleum oil was employed as a reference. The bio-oils caused no significant change in the vulcanization of rubber compounds cured using peroxide. However, the compounds containing bio-oils and cured with sulfur showed a faster vulcanization than the ones with DAE. The bio-oils strongly affected the crosslink density of rubber compounds in both curing systems. The use of bio-oils caused a low crosslink density due to the possible implication of curing agents to bio-oil molecules. The properties of rubber compounds dependent on the different levels of crosslink density were also investigated. The results revealed that when the crosslink density increased, the modulus, tensile strength, and hardness of the rubber compounds increased and the elongation at break and compression set decreased. The use of bio-oils in the rubber compounds cured with different curing systems gave low modulus at 300% strain, tensile strength, and hardness but high elongation at break and compression set when compared to the ones with DAE. However, no significant change was observed for the compression set of the rubber compounds cured using sulfur. With the presence of bio-oils, the properties of rubber compounds cured with sulfur system deteriorated less than those of the ones cured with peroxide.


Introduction
Given that raw rubber does not retain its shape nor retract to its original form after a large deformation, it requires vulcanization to become useful. Vulcanization is a chemical reaction that occurs under high temperatures of 120 • C-200 • C to induce bonding among rubber chain segments and generate a 3D network structure (crosslinking point) within the rubber matrix. This process generates a rubber material with the desired shape and size. Two types of vulcanization or curing systems, i.e., sulfur and peroxide curing systems, are widely used in unsaturated rubber compounds. The crosslink types formed after vulcanization vary with the vulcanization system. The rubber compounds cured with sulfur contain long rubber chains that are covalently linked via sulfide bridges ranging from monoand di-to poly-sulfidic bridges. As a curing agent, peroxide forms a radical on the rubber chains, and two rubber radicals bind to form the -C-C-crosslink. Compared with the sulfur crosslink, the-C-C-bond of the peroxide curing system is rigid and strong. Thus, the sulfur curing system shows flexibility. However, the thermal stability of -C-C-bond is higher than that of the sulfur crosslink, resulting in good heat resistance and a low compression set.

Preparation of NR Compounds
Sulfur-cured rubber compounds were prepared as previously described [16]. For peroxide-cured rubber compounds, unfilled NR compounds containing different types of processing oils, i.e., DAE, PO, and SBO, were prepared as shown in Table 1. A two-step mixing procedure was adopted for the preparation of rubber compounds ( Figure 1). For the first step, the NR compounds containing oils were mixed using an internal mixer at the following conditions: fill factor of 0.8, initial temperature of 60 • C, and rotor speed of 55 rpm. NR was masticated for 2 min before the processing oils were added and mixed continuously for 2 min. The processing oils were added and mixed for 1 min. Afterward, the NR compounds were transferred to the internal mixer and sheeted by a two-roll mill. The NR compounds were kept for 24 h at room temperature before the curing agents were added. In the second step, the curing agents were mixed with the NR compounds using a two-roll mill. The NR compounds were then sheeted by a two-roll mill and kept for 24 h at room temperature before further characterizations.

Swelling Test
Samples of NR compounds without processing oil cured by DCP at 170 °C were prepared and cut into sheets with a size of approximately 1 cm × 1 cm × 0.2 cm. The swelling of NR vulcanizates in different types of oils was tested. The samples were immersed in oil with a fixed volume of 30 mL for 30 days. The percentage of the swelling of the samples was calculated using Equation (1): where w0 and w1 are the weights of a sample before and after swelling in oil, respectively.

Cure Behavior
The cure characteristics of NR compounds were measured using a moving die rheometer in accordance with ASTM D5289 at various isothermal temperatures, i.e., 170 °C, 180 °C, 190 °C, and 200 °C. Scorch and cure times were calculated by using different percentages of cure, in which the scorch time was considered at 10% cure and cure time at 90% cure. The cure rate index, which is equal to [100/(cure time-scorch time)], was also calculated. For the testing of properties, i.e., crosslink density, mechanical properties, hardness, and compression set, all rubber compounds were vulcanized to their cure times by compression molding at 170 °C.

Crosslink Density
The crosslink density of NR vulcanizates was investigated by the equilibrium swelling method. Samples prepared with a fixed size of 10 mm × 10 mm × 2 mm were swollen in 20 mL of toluene at a room temperature. After swelling for 7 days, the samples were dried at 105 °C for 24 h. The volume fraction of polymers in the swollen rubber (Vr) was determined using Equation (2), and crosslink density (Xc) was calculated using Equation where m1 is the weight of polymer, m2 is the weight of solvent in the swollen NR vulcanizate at equilibrium swelling, ρ1 is the density of rubber vulcanizates before swelling, and ρ2 is the density of solvent.
where X is the polymer-solvent interaction parameter (0.391) and V2 is the molar volume of the solvent (106.3 cm 3 /mol).

Tensile Properties
The tensile properties, i.e., modulus at 300% strain, tensile strength, and elongation at break, were tested using a universal testing machine (Tinius Olsen, Tinius Olsen TMC, Horsham, PA, USA). The rubber vulcanizates were cut to a dumbbell shape specimen by using a die cut type I of ISO37 standard. The specimens were tested at room temperature with an extension speed of 500 mm/min.  Samples of NR compounds without processing oil cured by DCP at 170 • C were prepared and cut into sheets with a size of approximately 1 cm × 1 cm × 0.2 cm. The swelling of NR vulcanizates in different types of oils was tested. The samples were immersed in oil with a fixed volume of 30 mL for 30 days. The percentage of the swelling of the samples was calculated using Equation (1): where w 0 and w 1 are the weights of a sample before and after swelling in oil, respectively.

Cure Behavior
The cure characteristics of NR compounds were measured using a moving die rheometer in accordance with ASTM D5289 at various isothermal temperatures, i.e., 170 • C, 180 • C, 190 • C, and 200 • C. Scorch and cure times were calculated by using different percentages of cure, in which the scorch time was considered at 10% cure and cure time at 90% cure. The cure rate index, which is equal to [100/(cure time-scorch time)], was also calculated. For the testing of properties, i.e., crosslink density, mechanical properties, hardness, and compression set, all rubber compounds were vulcanized to their cure times by compression molding at 170 • C.

Crosslink Density
The crosslink density of NR vulcanizates was investigated by the equilibrium swelling method. Samples prepared with a fixed size of 10 mm × 10 mm × 2 mm were swollen in 20 mL of toluene at a room temperature. After swelling for 7 days, the samples were dried at 105 • C for 24 h. The volume fraction of polymers in the swollen rubber (V r ) was determined using Equation (2), and crosslink density (X c ) was calculated using Equation (3) [17]: where m 1 is the weight of polymer, m 2 is the weight of solvent in the swollen NR vulcanizate at equilibrium swelling, ρ 1 is the density of rubber vulcanizates before swelling, and ρ 2 is the density of solvent.
where X is the polymer-solvent interaction parameter (0.391) and V 2 is the molar volume of the solvent (106.3 cm 3 /mol).

Tensile Properties
The tensile properties, i.e., modulus at 300% strain, tensile strength, and elongation at break, were tested using a universal testing machine (Tinius Olsen, Tinius Olsen TMC, Horsham, PA, USA). The rubber vulcanizates were cut to a dumbbell shape specimen by using a die cut type I of ISO37 standard. The specimens were tested at room temperature with an extension speed of 500 mm/min. The hardness of rubber vulcanizates containing different types of processing oils and cured by sulfur and peroxide was tested using a durometer (Frank GmbH, Hamburg, Germany) in accordance with the ASTM D2240 test procedure, and the results are expressed in Shore A.

Compression Set
The compression set of rubber compounds containing different types of processing oils was tested in accordance with ASTM D395. The rubber vulcanizates were compressed for 25% deformation and heated in a hot air oven (Memmert, ITS Co., Ltd., Bangkok, Thailand) at 100 • C for 22 h. After heating, the rubber vulcanizates were released from the compression to restore their original shape for 30 min. The compression set of the rubber vulcanizates was calculated as shown in Equation (4): where t 0 is the thickness of the samples; t 1 is the thickness of the samples after testing; t s is the thickness of the spacer bar. The properties of rubber compounds, such as swelling in oils, crosslink density, modulus, tensile strength, elongation at break, hardness, and compression set, were tested in three samples. The average value and standard deviation were calculated and reported.

Solubility Aspects
Given the different chemical structures of rubber and oil, the compatibility of these components depends on the solubility parameter (δ). A solubility parameter difference of oil and rubber close to zero, i.e., |δ oil − δ rubber |→ 0, promotes their compatibility. The solubility parameter can be calculated from the volume of substance per mole and the molar attraction constant related to cohesive energy (E coh ) using the equation described by Small [18,19]. The solubility parameters of NR and DAE oil were 16.9 and 17.5 J 1/2 /cm 3/2 , respectively [12], and the difference in their solubility parameter was 0.6 J 1/2 /cm 3/2 . The solubility parameters of bio-oils, i.e., PO and SBO, were reported. The solubility parameters of PO are 18.3 and 18.4 J 1/2 /cm 3/2 [20][21][22], whereas those of SBO are 16.2 and 16.8 J 1/2 /cm 3/2 [20,23,24]. The chemical structure of bio-oils, i.e., PO and SBO, comprises three fatty acids attached to a glycerol backbone via an ester linkage ( Figure 2). Bio-oils also contain slight amounts of free fatty acids [25], which are also released by the hydrolysis of triglycerides [26]. The major fatty acids in PO are oleic-, palmitic-, lenolenic-, and stearicacids, while as the major fatty acids in SBO are linoleic-, oleic-, palmitic-, lenolenic-, and stearic-acids [15,[27][28][29][30]. The unsaturated/saturated ratio of fatty acids in PO and SBO is in the range of 1.04-1.32 and 5.35-6.14, respectively. Thus, the calculation of actual solubility parameter of bio-oil is complicated. The swelling of NR in the different types of oils was applied to investigate the compatibility of these components ( Figure 3). The results revealed that both bio-oils, i.e., PO and SBO, showed higher percentage of swelling than DAE. Thus, these bio-oils promote the compatibility with NR molecule. cured by sulfur and peroxide was tested using a durometer (Frank GmbH, Hamburg, Germany) in accordance with the ASTM D2240 test procedure, and the results are expressed in Shore A.

Compression Set
The compression set of rubber compounds containing different types of processing oils was tested in accordance with ASTM D395. The rubber vulcanizates were compressed for 25% deformation and heated in a hot air oven (Memmert, ITS Co., Ltd., Bangkok, Thailand) at 100 °C for 22 h. After heating, the rubber vulcanizates were released from the compression to restore their original shape for 30 min. The compression set of the rubber vulcanizates was calculated as shown in Equation (4): where t0 is the thickness of the samples; t1 is the thickness of the samples after testing; ts is the thickness of the spacer bar. The properties of rubber compounds, such as swelling in oils, crosslink density, modulus, tensile strength, elongation at break, hardness, and compression set, were tested in three samples. The average value and standard deviation were calculated and reported.

Solubility Aspects
Given the different chemical structures of rubber and oil, the compatibility of these components depends on the solubility parameter (δ). A solubility parameter difference of oil and rubber close to zero, i.e., |δoil − δrubber|→ 0, promotes their compatibility. The solubility parameter can be calculated from the volume of substance per mole and the molar attraction constant related to cohesive energy (Ecoh) using the equation described by Small [18,19]. The solubility parameters of NR and DAE oil were 16.9 and 17.5 J 1/2 /cm 3/2 , respectively [12], and the difference in their solubility parameter was 0.6 J 1/2 /cm 3/2 . The solubility parameters of bio-oils, i.e., PO and SBO, were reported. The solubility parameters of PO are 18.3 and 18.4 J 1/2 /cm 3/2 [20][21][22], whereas those of SBO are 16.2 and 16.8 J 1/2 /cm 3/2 [20,23,24]. The chemical structure of bio-oils, i.e., PO and SBO, comprises three fatty acids attached to a glycerol backbone via an ester linkage ( Figure 2). Bio-oils also contain slight amounts of free fatty acids [25], which are also released by the hydrolysis of triglycerides [26]. The major fatty acids in PO are oleic-, palmitic-, lenolenic-, and stearic-acids, while as the major fatty acids in SBO are linoleic-, oleic-, palmitic-, lenolenic-, and stearic-acids [15,[27][28][29][30]. The unsaturated/saturated ratio of fatty acids in PO and SBO is in the range of 1.04-1.32 and 5.35-6.14, respectively. Thus, the calculation of actual solubility parameter of bio-oil is complicated. The swelling of NR in the different types of oils was applied to investigate the compatibility of these components ( Figure 3). The results revealed that both bio-oils, i.e., PO and SBO, showed higher percentage of swelling than DAE. Thus, these bio-oils promote the compatibility with NR molecule.    Figure 4 shows a typical torque-time curve of NR compounds containing p oils with peroxide curing systems and compared with those using sulfur curin from [16]. The curing system showed a strong influence on the cure curve behav NR compounds throughout the curing period in this study. The results reveale cure curves of the peroxide-cured NR compounds containing processing oil marching behavior, and those of the sulfur-cured NR compounds exhibited a behavior. The behaviors of cure curves in the over curing period depend on the tion between the formation and breakage of the crosslinking points within the ru trix. Given the different thermal stabilities of crosslinking points, the thermal s C-C in the peroxide curing system was higher than that of sulfidic crosslinks. dissociation energy of crosslinking points of rubber compounds was in the ord (343.2 kJ/mol) > C-S (276.2 kJ/mol) > S-S (205.1 kJ/mol) [1]. Therefore, during curing period, the crosslinks of the sulfur-cured NR compounds decomposed m than those of the peroxide-cured NR compounds. Generally, this condition c sulfur-cured NR compounds to show a reversion behavior during the over curin On the other hand, the cure curves at high temperatures, especially at 200 °C, of t compounds cured with peroxide showed reversion behavior. This is due to the tion of NR molecules and the reduction of crosslinking points within the rubber   Figure 4 shows a typical torque-time curve of NR compounds containing processing oils with peroxide curing systems and compared with those using sulfur curing system from [16]. The curing system showed a strong influence on the cure curve behavior of the NR compounds throughout the curing period in this study. The results revealed that the cure curves of the peroxide-cured NR compounds containing processing oil showed a marching behavior, and those of the sulfur-cured NR compounds exhibited a reversion behavior. The behaviors of cure curves in the over curing period depend on the competition between the formation and breakage of the crosslinking points within the rubber matrix. Given the different thermal stabilities of crosslinking points, the thermal stability of C-C in the peroxide curing system was higher than that of sulfidic crosslinks. The bond dissociation energy of crosslinking points of rubber compounds was in the order of C-C (343.2 kJ/mol) > C-S (276.2 kJ/mol) > S-S (205.1 kJ/mol) [1]. Therefore, during the over curing period, the crosslinks of the sulfur-cured NR compounds decomposed more easily than those of the peroxide-cured NR compounds. Generally, this condition caused the sulfur-cured NR compounds to show a reversion behavior during the over curing period. On the other hand, the cure curves at high temperatures, especially at 200 • C, of the rubber compounds cured with peroxide showed reversion behavior. This is due to the degradation of NR molecules and the reduction of crosslinking points within the rubber matrix. Figure 5A-C illustrate the cure characteristics, such as scorch time, cure time, and cure rate index, respectively, of NR compounds containing processing oils from different curing systems. Owing to the effect of different curing systems, the scorch time of NR compounds under peroxide curing was shorter than that under sulfur curing. This finding may be attributed to the different reactions of premature vulcanization. By contrast, the use of sulfur curing system led to a shorter cure time than the use of peroxide curing system Figure 5A-C illustrate the cure characteristics, such as scorch time, cure time, and cure rate index, respectively, of NR compounds containing processing oils from differen curing systems. Owing to the effect of different curing systems, the scorch time of NR compounds under peroxide curing was shorter than that under sulfur curing. This finding may be attributed to the different reactions of premature vulcanization. By contrast, the use of sulfur curing system led to a shorter cure time than the use of peroxide curing system due to the different behaviors during the over curing period, i.e., marching fo  The processing oils did not significantly influence the scorch and cure times of the NR compounds using peroxide curing system, which was in contrast with the sulfurcured NR compounds. The different types of processing oils strongly affected the cure time of sulfur-cured NR compounds, in which the NR compounds containing bio-oils, i.e., PO and SBO, had a shorter cure time compared with the one with DAE oil. For bio-oil compositions containing certain amounts of free fatty acids, these fatty acids can react with ZnO, enhancing the speed of vulcanization reaction. Thus, the sulfur-cured NR compounds containing both bio-oils, i.e., PO and SBO, showed a shorter cure time and higher cure rate index than the one containing DAE oil [16]. However, the similar levels on the cure time and cure rate index of the rubber compounds were observed when the high temperatures were applied.

Cure Kinetics
The cure kinetics [31], i.e., cure reaction rate constant and activation energy, of the rubber compounds were calculated. Figure 6 shows the typical plot of ln(MH − Mt) against t of the rubber compounds containing processing oils with different curing systems. The slope of the line for the rubber compounds containing processing oils and cured with sulfur was steeper than that for the rubber compounds containing processing oils and cured using peroxide. Figure 7 shows the cure reaction rate constant of the rubber compounds as determined by the slope of these lines. The different types of processing oils had no influence on the cure behavior of rubber compounds cured with peroxide. Thus, the cure reaction rate constant of these compounds showed no significant change. In addition, results showed that the cure reaction rate constant increases with increasing temperatures. As discussed earlier, the fatty acids in bio-oils can speed up sulfur vulcanization. The cure reaction rate constant of the rubber compounds containing bio-oils and cured with sulfur was higher than that of the compounds containing DAE oil [16]. The processing oils did not significantly influence the scorch and cure times of the NR compounds using peroxide curing system, which was in contrast with the sulfurcured NR compounds. The different types of processing oils strongly affected the cure time of sulfur-cured NR compounds, in which the NR compounds containing bio-oils, i.e., PO and SBO, had a shorter cure time compared with the one with DAE oil. For bio-oil compositions containing certain amounts of free fatty acids, these fatty acids can react with ZnO, enhancing the speed of vulcanization reaction. Thus, the sulfur-cured NR compounds containing both bio-oils, i.e., PO and SBO, showed a shorter cure time and higher cure rate index than the one containing DAE oil [16]. However, the similar levels on the cure time and cure rate index of the rubber compounds were observed when the high temperatures were applied.

Cure Kinetics
The cure kinetics [31], i.e., cure reaction rate constant and activation energy, of the rubber compounds were calculated. Figure 6 shows the typical plot of ln(M H − M t ) against t of the rubber compounds containing processing oils with different curing systems. The slope of the line for the rubber compounds containing processing oils and cured with sulfur was steeper than that for the rubber compounds containing processing oils and cured using peroxide. Figure 7 shows the cure reaction rate constant of the rubber compounds as determined by the slope of these lines. The different types of processing oils had no influence on the cure behavior of rubber compounds cured with peroxide. Thus, the cure reaction rate constant of these compounds showed no significant change. In addition, results showed that the cure reaction rate constant increases with increasing temperatures. As discussed earlier, the fatty acids in bio-oils can speed up sulfur vulcanization. The cure reaction rate constant of the rubber compounds containing bio-oils and cured with sulfur was higher than that of the compounds containing DAE oil [16]. Figure 8A,B present the plot of lnk versus 1/T and the activation energy of the rubber compounds containing processing oils and cured by peroxide and sulfur, respectively. The activation energy was obtained by the slope of the plot of lnk versus 1/T [31]. No significant difference was observed in the activation energies of the rubber compounds containing different types of processing oils and cured with DCP. However, the results showed different behaviors to those of the rubber compounds cured with sulfur. These results revealed that the use of bio-oils in the rubber compounds cured with sulfur decreased the activation energy. This observation supported the proposition that bio-oils accelerate

Crosslink Density
The degree of crosslinking points within the rubber matrix as a crosslink density is a crucial factor in optimizing end-use properties, such as hardness, modulus, tensile strength, tear strength, and abrasion resistance [1]. As shown in the cure curve of rubber compounds in Figure 4, torque difference, i.e., maximum torque (M H )−minimum torque (M L ), is widely applied to indicate the crosslink density of rubber compounds due to an increase in the torque of unfilled rubber compounds during vulcanization. This increase is affected by the increase in crosslink point within the rubber matrix. Figure 9A shows the torque difference as a function of curing temperatures of NR compounds containing different processing oils and cured by various curing systems. It was found that the biooils strongly affected the torque difference of rubber compounds cured by peroxide. The results showed that the torque difference of DCP-cured rubber compounds decreased with the addition of bio-oils. Thus, the use of bio-oils decreases the crosslink density of the DCP-cured rubber compounds. The crosslink density can be measured with equilibrium swelling in toluene and calculated using the Flory-Rehner equation. The crosslink density of the NR compounds containing different types of processing oil were highly correlated with the torque difference obtained from the cure curve ( Figure 9B). Among the different types of processing oil, the DAE oil showed a higher crosslink density than the bio-oils in an identical curing system. The addition of bio-oils in the NR compound decreased the crosslink density, in which PO induced a higher level of crosslink density than SBO.  Figure 8A,B present the plot of lnk versus 1/T and the activation energy of the ru compounds containing processing oils and cured by peroxide and sulfur, respecti The activation energy was obtained by the slope of the plot of lnk versus 1/T [31] significant difference was observed in the activation energies of the rubber compou containing different types of processing oils and cured with DCP. However, the re showed different behaviors to those of the rubber compounds cured with sulfur. T results revealed that the use of bio-oils in the rubber compounds cured with sulfu creased the activation energy. This observation supported the proposition that bio accelerate sulfur vulcanization-a short cure time occurs with the increase in cure index and cure reaction rate constant [16]. For the peroxide curing system, peroxide radicals are able to abstract a hydrogen atom from polymer chains and any available source, such as antioxidant or processing oil, in the component contained in the rubber compound system. After the peroxide radical abstracts the hydrogen atom from non-polymer chains, such as oil, the crosslink density within the rubber matrix is reduced. Therefore, chemical structure is a main factor influencing the efficiency of abstraction by a radical. The abstraction of allylic hydrogen by a radical has a higher efficiency than that with tertiary, secondary, and primary structures [1]. The structure of bio-oils used in this study, i.e., PO and SBO, consists of three fatty acids attached to a glycerol via an ester linkage. Fatty acids can either be saturated or unsaturated aliphatic hydrocarbons depending on the type. SBO contains more unsaturated fatty acids than PO, as indicated by the ratio of unsaturated and saturated fatty acids. Therefore, the addition of SBO in the NR compounds decreased the crosslink density because of the high efficiency of SBO in the reaction with peroxide curing agent.

Crosslink Density
The degree of crosslinking points within the rubber matrix as a crosslink density is a crucial factor in optimizing end-use properties, such as hardness, modulus, tensile strength, tear strength, and abrasion resistance [1]. As shown in the cure curve of rubber compounds in Figure 4, torque difference, i.e., maximum torque (MH)−minimum torque (ML), is widely applied to indicate the crosslink density of rubber compounds due to an increase in the torque of unfilled rubber compounds during vulcanization. This increase is affected by the increase in crosslink point within the rubber matrix. Figure 9A shows the torque difference as a function of curing temperatures of NR compounds containing different processing oils and cured by various curing systems. It was found that the biooils strongly affected the torque difference of rubber compounds cured by peroxide. The results showed that the torque difference of DCP-cured rubber compounds decreased with the addition of bio-oils. Thus, the use of bio-oils decreases the crosslink density of the DCP-cured rubber compounds. The crosslink density can be measured with equilibrium swelling in toluene and calculated using the Flory-Rehner equation. The crosslink density of the NR compounds containing different types of processing oil were highly correlated with the torque difference obtained from the cure curve ( Figure 9B). Among the different types of processing oil, the DAE oil showed a higher crosslink density than the bio-oils in an identical curing system. The addition of bio-oils in the NR compound decreased the crosslink density, in which PO induced a higher level of crosslink density than SBO.
For the peroxide curing system, peroxide radicals are able to abstract a hydrogen atom from polymer chains and any available source, such as antioxidant or processing oil, in the component contained in the rubber compound system. After the peroxide radical abstracts the hydrogen atom from non-polymer chains, such as oil, the crosslink density within the rubber matrix is reduced. Therefore, chemical structure is a main factor influencing the efficiency of abstraction by a radical. The abstraction of allylic hydrogen by a radical has a higher efficiency than that with tertiary, secondary, and primary structures [1]. The structure of bio-oils used in this study, i.e., PO and SBO, consists of three fatty acids attached to a glycerol via an ester linkage. Fatty acids can either be saturated or unsaturated aliphatic hydrocarbons depending on the type. SBO contains more unsaturated fatty acids than PO, as indicated by the ratio of unsaturated and saturated fatty acids. Therefore, the addition of SBO in the NR compounds decreased the crosslink density because of the high efficiency of SBO in the reaction with peroxide curing agent. Among the different curing systems, the sulfur-cured rubber compounds showed similar behavior on crosslink density when compared to the ones cured with DCP. In general, the sulfur used as a curing agent for rubber is active toward the carbon double bond (-C=C-) of unsaturated fatty acids [16,32,33]. This property possibly explains the reduction of crosslink density in the sulfur-cured NR compounds with bio-oils. The proposed model for the representation of bio-oils, i.e., PO and SBO, in the rubber compounds cured with different curing systems was shown in Figure 10.  Among the different curing systems, the sulfur-cured rubber compounds showed similar behavior on crosslink density when compared to the ones cured with DCP. In general, the sulfur used as a curing agent for rubber is active toward the carbon double bond (-C=C-) of unsaturated fatty acids [16,32,33]. This property possibly explains the reduction of crosslink density in the sulfur-cured NR compounds with bio-oils. The proposed model for the representation of bio-oils, i.e., PO and SBO, in the rubber compounds cured with different curing systems was shown in Figure 10.

Tensile Properties, Hardness, and Compression Set of NR Compounds
As discussed in the section of solubility aspects, bio-oils have promoted comp with the NR matrix compared with the DAE oil. However, the rubber compoun taining bio-oils did not show superior properties. In this study, the use of differen of oils strongly influenced the crosslink density. Therefore, the correlation of cr density and properties of rubber compounds containing different types of oils was investigated. Mechanical properties, including modulus at 300% strain, tensile s and elongation at break, were tested for the rubber compounds containing oils an with different curing systems. The results are shown in Figure 11A-C. The rubb pounds containing different types of oils and cured by sulfur showed a lower mod 300% strain and higher tensile strength and elongation at break than the rubb pounds cured by DCP. This observation confirmed that the rubber compounds cur sulfur were more flexible than those cured with DCP. The mechanical properties of compounds containing different types of oils were presented as a function of cr density. The modulus at 300% strain and tensile strength of the rubber compoun taining different types of oils cured with DCP increased with the crosslink dens the elongation at break decreased. These results revealed that the crosslink density the rubber matrix strongly affected the mechanical properties of rubber compou addition to the crosslink density, the viscosity of the processing oils affected the pro of the rubber compounds, especially elongation at break. It was reported that th bio-oils gave higher elongation at break than the ones with DAE. This was due to viscosity of bio-oils that promotes a high lubricating effect. So, it could be suppor

Tensile Properties, Hardness, and Compression Set of NR Compounds
As discussed in the section of solubility aspects, bio-oils have promoted compatibility with the NR matrix compared with the DAE oil. However, the rubber compounds containing bio-oils did not show superior properties. In this study, the use of different types of oils strongly influenced the crosslink density. Therefore, the correlation of crosslink density and properties of rubber compounds containing different types of oils was further investigated. Mechanical properties, including modulus at 300% strain, tensile strength, and elongation at break, were tested for the rubber compounds containing oils and cured with different curing systems. The results are shown in Figure 11A-C. The rubber compounds containing different types of oils and cured by sulfur showed a lower modulus at 300% strain and higher tensile strength and elongation at break than the rubber compounds cured by DCP. This observation confirmed that the rubber compounds cured with sulfur were more flexible than those cured with DCP. The mechanical properties of rubber compounds containing different types of oils were presented as a function of crosslink density. The modulus at 300% strain and tensile strength of the rubber compounds containing different types of oils cured with DCP increased with the crosslink density, but the elongation at break decreased. These results revealed that the crosslink density within the rubber matrix strongly affected the mechanical properties of rubber compounds. In addition to the crosslink density, the viscosity of the processing oils affected the properties of the rubber compounds, especially elongation at break. It was reported that the use of bio-oils gave higher elongation at break than the ones with DAE. This was due to the low viscosity of bio-oils that promotes a high lubricating effect. So, it could be supported the results in this study that the use of two types of bio-oils, i.e., PO and SBO, in the rubber compounds showed a high elongation at break [34].
increased elongation at break. The change in the modulus of rubber compounds cured with sulfur and peroxide system was nearly similar. However, it was observed that the decrease in tensile strength of rubber compounds cured with sulfur system was less than the ones cured with peroxide. As mentioned, the presence of bio-oils showed a positive effect on elongation at break. It was noted that the increase in elongation at break of rubber compounds cured with sulfur system was higher than the ones cured with peroxide. For rubber formulations used here, it can be inferred that the use of bio-oils is more suitable for sulfur than peroxide curing system.  The hardness of rubber compounds containing different types of oils and cured with various curing systems was in Figure 12A. The rubber compounds cured by peroxide curing system exhibited a slightly lower hardness than those cured with sulfur. The hardness of rubber compounds changed when different types of oils were used. As discussed earlier, the addition of bio-oils in the rubber compounds decreased the levels of crosslink density. The rubber compounds containing bio-oils showed a lower hardness than the compounds containing DAE oil under the same curing system. As shown in Figure 12A, the hardness of rubber compounds slightly increased with the crosslink density. In addition, the bio-oils promoted a good lubricating effect due to the low viscosity. Because the As can be seen in Figure 11A-C, the rubber compounds cured with DCP showed the same trend of the mechanical properties with rubber compounds cured with sulfur. This evidence confirmed that the crosslink density within the rubber matrix gave a huge influence on the mechanical properties. As can be seen in Table 2, regardless of curing system, the replacement of DAE with bio-oils produced a similar change in the tensile properties of rubber compounds, including the decreased modulus and tensile strength but increased elongation at break. The change in the modulus of rubber compounds cured with sulfur and peroxide system was nearly similar. However, it was observed that the decrease in tensile strength of rubber compounds cured with sulfur system was less than the ones cured with peroxide. As mentioned, the presence of bio-oils showed a positive effect on elongation at break. It was noted that the increase in elongation at break of rubber compounds cured with sulfur system was higher than the ones cured with peroxide. For rubber formulations used here, it can be inferred that the use of bio-oils is more suitable for sulfur than peroxide curing system. The hardness of rubber compounds containing different types of oils and cured with various curing systems was in Figure 12A. The rubber compounds cured by peroxide curing system exhibited a slightly lower hardness than those cured with sulfur. The hardness of rubber compounds changed when different types of oils were used. As discussed earlier, the addition of bio-oils in the rubber compounds decreased the levels of crosslink density. The rubber compounds containing bio-oils showed a lower hardness than the compounds containing DAE oil under the same curing system. As shown in Figure 12A, the hardness of rubber compounds slightly increased with the crosslink density. In addition, the bio-oils promoted a good lubricating effect due to the low viscosity. Because the low crosslink density and good lubrication effect, the use of bio-oils showed low hardness of the rubber compounds when compared to the ones with DAE.
is compressed at specific deformation, time, and temperature. Figure 12B shows the compression set of rubber compounds containing different types of oils and cured in various curing systems. The results revealed that the compression set of the rubber compounds was strongly affected by the curing systems. The rubber compounds cured by the peroxide curing system showed a lower compression set than those cured by the sulfur system. This finding was due to the good thermal stability of the -C-C-bond generated by the peroxide curing system, leading to a low compression set. The compression set of rubber compounds containing different types of oils was considered as a function of crosslink density. For the rubber compounds cured with peroxide, the different types of oils induced significant differences in the compression set of NR compounds. The compression set of the rubber compounds decreased with the increase in the crosslink density ( Figure  12B). This result was due to the high crosslink density that limited the mobility of rubber chains. Thus, the crosslinked network prevented rubber deformation. However, the compression set did not significantly change when different types of oils were used in the rubber compounds cured by the sulfur curing system.

Conclusions
The influences of bio-oils, i.e., PO and SBO, on the properties of the unfilled NR compounds cured with peroxide system were investigated here and comparatively discussed with the ones cured with sulfur system from our previous study using DAE-based petroleum oil as a reference. When compared with DAE, the bio-oils did not significantly change the cure time, cure rate index, cure reaction rate constant, and activation energy of the rubber compounds cured by peroxide. However, NR compounds containing bio-oils cured with sulfur showed a shorter cure time, higher cure rate index and cure reaction rate constant, and a lower activation energy than the compounds with DAE. The bio-oils Compression set is also an important property of rubber compounds and is defined as the amount of permanent deformation of rubbers that occurs when the rubber material is compressed at specific deformation, time, and temperature. Figure 12B shows the compression set of rubber compounds containing different types of oils and cured in various curing systems. The results revealed that the compression set of the rubber compounds was strongly affected by the curing systems. The rubber compounds cured by the peroxide curing system showed a lower compression set than those cured by the sulfur system. This finding was due to the good thermal stability of the -C-C-bond generated by the peroxide curing system, leading to a low compression set. The compression set of rubber compounds containing different types of oils was considered as a function of crosslink density. For the rubber compounds cured with peroxide, the different types of oils induced significant differences in the compression set of NR compounds. The compression set of the rubber compounds decreased with the increase in the crosslink density ( Figure 12B). This result was due to the high crosslink density that limited the mobility of rubber chains. Thus, the