Evaluation of Dynamic Materials Procured from Waste Biomass

Methyl acrylate (MA) monomer was graft copolymerized onto Hibiscus sabdariffa stem fiber and used to explore the additive effect of vinyl acrylate (VA) and ethyl acrylate (EA) on percentage grafting and the properties of the fiber, in binary vinyl monomeric mixtures. The graft copolymers were reinforced into phenol-formaldehyde polymer matrix to form biocomposites and characterized by FTIR, XRD, TGA, DTA, and SEM techniques. They were evaluated for physico-chemical changes in properties like moisture absorption at different relative humidity levels and chemical resistance against 1 N NaOH and 1 N HCl. These graft copolymers-reinforced biocomposites had higher mechanical strength like hardness, modulus of rupture, modulus of elasticity, and stress at the limit of proportionality. These novel materials can have numerous scientific and industrial applications for the development of technology.


Introduction
Graft copolymerization is a magnificent technique for incorporating the desired properties into raw fiber without drastically affecting its basic traits. It imparts additional features such as thermal and chemical resistance to the naturally existing backbone for their use in various fields. Natural fibers such as ramie, flax, jute, and pine needle are the most suitable reinforcement materials because of their relatively high strength and stiffness for their use in industries such as automobile, packaging, and construction materials that fulfill the economic and ecological requirements.
Composites are the wonder materials, which after meeting the challenges of aerospace have cascaded down for catering the domestic and industrial avenues. Phenoplasts have a wide range of applications as lacquer, varnish, molding compounds, laminate for wall panel, and table top. In the recent times many successful efforts have been made to prepare phenol-formaldehyde composites and to increase its mechanical potential by using different reinforcements like wood particle, hemp scotch, banana fiber, and cellulose fiber [1][2][3][4][5][6].
Hibiscus sabdariffa (Roselle) is a rich source of cellulose found in abundance throughout the world and has attained prominence as a jute substitute, and attempts are being made to extend its cultivation in areas which are not favorable for jute cultivation. It shows better mechanical properties when studied for injection-molded isotactic polypropylene/Roselle fiber composites [7,8]. The versatility of this magnificent chemical technique inspired the thoughts to implement it onto Hibiscus sabdariffa stem fiber by using effective methyl acrylate as principal monomer and explore its cumulative effect in binary vinyl monomer mixture and on the properties of the fiber using ethyl acrylate and vinyl acrylate as secondary monomer and to use the raw fiber, graft copolymers as reinforcement in phenol-formaldehyde polymer matrix-based composite that remains unexplored.   IR spectra of the H. sabdariffa and its graft copolymers were recorded with Perkin Elmer Fourier Transform Infrared (FTIR) spectrophotometer using KBr pellets (Sigma Aldrich). Scanning Electron Micrographs (SEMs) of H. sabdariffa and its graft copolymers were obtained by using Electron Microscopy Machine (LEO 435-25-20). Thermogravimetric and differential thermal analyses were performed on thermal analyzer (LINSEIS, L-81 11). Tensile and compressive strength was tested on Universal Testing Machine (HOUNSFIELD, H25KS).

Graft Copolymerization.
Graft copolymerization of the monomer onto H. sabdariffa was carried out for optimization of different reaction conditions like reaction time, reaction temperature, monomer concentration, concentration of initiator system, and pH in order to obtain maximum graft yield. The fiber (0.5 g) was activated by swelling in 100 mL of the distilled water for 24 hrs. Mixture of ceric ammonium nitrate (CAN) and concentrated HNO 3 was slowly added to the reaction medium with continuous stirring followed by the drop-by-drop addition of a definite ratio of binary vinyl monomeric mixture. The reaction was carried out at a definite temperature for a particular time interval. On completion of the reaction, poly(MA), poly(MA-co-VA) and poly(MA-co-EA) were removed on extraction with acetone, methanol, chloroform, and water. The graft copolymer was dried at 50 • C, till a constant weight was obtained. The percent grafting (P g ) was calculated as per the method reported by [1] where W f is the final weight of the fiber and W i is the initial weight of the fiber.

Synthesis of Phenol-Formaldehyde Resin.
Phenol-formaldehyde resin was prepared in a resin kettle by taking specific molar ratio of phenol and formalin. Phenol and   formalin were mixed with the help of mechanical stirrer. Sodium hydroxide solution (50% aqueous solution of sodium hydroxide prepared on the basis of 5% relative weight of sodium hydroxide to the weight of phenol taken) was added to the reaction mixture with constant stirring and heating. Since the reaction was exothermic, the reaction temperature was maintained between 50 • and 60 • C by circulating the cold water around the resin kettle initially for two hours. Thereafter, reaction temperature was raised to 80-90 • C, and setting of resinification was checked on appearance of turbidity by adding a drop of condensing resin to the cold water. Condensing resin was further heated at this temperature for another two and half hours, and afterwards the resin was cooled to room temperature [9].   ungrafted, and composite samples in a humidity chamber for about twelve hours and then the final weight (W f ) of the samples exposed to different relative humidities ranging from 30 to 90% was taken. The % moisture absorbance was calculated from the increase in initial weight in the following manner [10]:

Acid and Base
Resistance. Acid and base resistance studies were carried out as per the method reported in (3). Acid and base resistance was studied by placing a known weight (Wi) of dry grafted, ungrafted samples, and composite in fixed volume (50 mL) of 1 N HCl and 1 N NaOH, and the final weights (W f ) of the samples were noted after 72 hours [10]: where P is the peak load, L the length of the sample, b the width of the sample, and d the thickness of the sample.

Modulus of Elasticity. MOE was determined according
to ASTM D 790 standard and was calculated using the following equation [9] where P is the peak load, L the length of the sample, b the width of the sample, d the thickness of the sample, P 1 the load at the limit of proportionality, and y = rate of bending.

Stress at the Limit of Proportionality. Stress at the limit of proportionality was calculated by using [9]
where P 1 is the load at the limit of proportionality, L the length of the sample, b the width of the sample, and d the thickness of the sample.

Hardness.
Hardness of the composites was tested using Rockwell Hardness tester (Balancing Instrument and Equipments Miraj Pvt. Ltd., Model-TSM) following ASTM D785 standard, using B-scale 100 Kg as a major load and 10 Kg as a minor load with 1/16 inch indenter steel ball, and it was measured in HRB.

Results and Discussion
Ceric ammonium nitrate used as source of ceric ion in presence of concentrated nitric acid plays an important role during graft copolymerization. Because of the large-size [Ce-O-Ce] 6+ ion it is unable to form complex with the fiber, whereas in presence of HNO 3 more and more of Ce  (Table 1). However, many other factors also determine the graft yield like the type of fiber, swelling, number of active sites, the nature and amount of the solvent and temperature of polymerization strongly influencing the reactivity ratios.
In absence of monomer rich phase, the diluents will compete with the monomers for adsorption sites. The amount of adsorption will depend upon the total amount of surface area present, and this, in turn, is dependent upon the rate of stirring. Physical factors like mixing efficiency determine the melt temperature, the pressure, the rheological properties, solubility of the initiator and the monomer. Elevated temperature favors the degradation, reduces the initiator half-life, modifies the rate or specificity of the reaction, and influences the solubility and rheological parameters [12,13].

FTIR and SEM
. IR spectrum of the H. sabdariffa showed a broad peak at 3424.0 cm −1 (-OH group), and peaks at 2924.7 cm −1 , 1246.9 cm −1 , and 1032.0 cm −1 were observed due to -CH 2 , C-C, and C-O stretching, respectively. However, the additional peak was observed due to MA (>C=O peak) at 1738 cm −1 . In all the cases the incorporated groups of secondary monomers were seen at 1638.0 cm −1 (vinyl group) in Hs-g-poly(MA-co-VA) and 1735.0 cm −1 (>C=O group) in Hs-g-poly(MA-co-EA), respectively. In SEM, the cellulose was gold plated to have an impact. It is quite evident from Figures 1(a) and 1(b) that there has been a sufficient deposition of polyvinyl monomers onto fiber. Comparison of the scanning electron micrographs of the phenoplast with H. sabdariffa-reinforced PF composite reveals the distinction between the surfaces due to incorporation of the reinforced fiber (Figures 1(c) and 1(d)).

XRD Studies.
The XRD overlay of the PF resin and the Hs-reinforced PF resin is given in Figure 2, which shows a distinct change in crystallinity after fiber reinforcement.

Thermal Evaluation.
Thermogravimetric and differential thermal analysis studies were carried out at the heating rate of 10 • C/second. The TGA results of the PF composite (Table 2) showed 500 • C and 600 • C as the initial decomposition temperature and final decomposition temperature, respectively. The percentage weight loss during this decomposition was found to be 26.61% in the temperature range of 50-500 • C while it was 73.39% during the final decomposition in the temperature range of 500-600 • C. The higher initial and final decomposition temperature could be due to three-dimensional network structure of the thermoset. The DTA showed prominent exothermic peaks at 551 • C (150 μV) that correspond to the major decomposition due to irreversible decomposition of the crystallites between 500 and 600 • C as a function of temperature, respectively. The IDT, FDT of fiber-reinforced composites have increased due to strong fiber matrix interaction. The grafted monomer acts as coupling agent and elevates the decomposition temperature. Cellulose in H. sabdariffa degrades by dehydration, glycogen formation, and depolymerization. In case of H. sabdariffa, two-stage decomposition has been found: the former stage is attributed to loss by dehydration, volatilization processes, whereas the later stage is attributed to loss by depolymerization, delignification, and oxidation of the char [10,14]. The addition of graft copolymer as reinforcement further increased the thermal stability of the composites.

Moisture Absorption Study.
It was found that graft copolymerization of vinyl monomer onto H. sabdariffa has a great impact on the moisture absorbance behavior (Table 3). It has been observed that, with increase in graft yield, there was a decrease in percent moisture absorbance. This was due to blocking of sites vulnerable for moisture absorbance with vinyl monomer chains, thereby converting the fiber to be less sensitive to moisture [6,10]. The incorporation of graft copolymers in the phenoplast improved the fiber matrix interaction that decreased the pores and increased the strength by acting as coupling agent.

Acid and Base
Resistance. It has been observed that acid base resistance of the fiber increased with increase in percent grafting. This is due to the fact that poly(vinyl) chains grafted onto H. sabdariffa fiber have less affinity for 1 N HCl and 1 N NaOH as compared to free hydroxyl groups present in ungrafted fiber. Therefore, the resistance of fiber towards acid base was found to increase with the incorporation of poly(vinyl) chains on the active sites of the backbone (Table 3) [6]. The incorporation of graft copolymers in the phenoplast improved the fiber matrix interaction that increased the strength of the composite.

Mechanical Evaluation
6.1. MOR, MOE, SP, and Hardness. The results obtained after the mechanical evaluation of phenoplast, fiberreinforced composites, and grafted-fiber-reinforced biocomposites are given in Table 4. The results clearly show that grafted fiber has enhanced the mechanical strength of the composites.
Thus, it is evident from the results that H. sabdariffa fiber as reinforcement has improved the mechanical properties of the P-F composites. In most of the cases, graft copolymers of methyl acrylate and its binary mixtures were found to exhibit better mechanical behavior such as wear resistance, tensile strength, compressive strength, MOR, MOE, SP and hardness as compared to the raw fiber-reinforced P-F composites and the phenoplast. The better mechanical behavior could be accounted for by the functioning of the monomer as a coupling agent, better polymer matrix interaction, compatibility and orientation of the fiber. However, some deviation in the results could be justified by other governing factors for overall mechanical performance like nature and amount of matrix and fiber, orientation, distribution of the fiber with respect to the matrix axis, form of reinforcement used (woven or nonwoven, grafted or ungrafted), strength of the interfacial bond between the fiber and matrix, length of the fiber (continuous or discontinuous), and aspect ratio that on mere imbalance may lead to debonding and cracking [1,15,16].

Conclusion
H. sabdariffa stem fiber when grafted with methyl acrylate and its binary vinyl monomeric mixture in the presence of ceric ion initiator yielded novel regenerated graft copolymers. It is evident from the characterization and evaluation studies of the graft copolymers through different techniques that grafting resulted in the morphological transformation that improved the various physico-chemicothermal properties of the H. sabdariffa fiber. The use of Hibiscus sabdariffa and its graft copolymers as reinforcement in polymer matrix-based composites has improved the mechanical strength of these bio-composites. The use of renewable waste biomass as graft copolymers and as reinforcement to form bio-composites can have numerous scientific and industrial applications. These advanced materials can be used in transportation, packaging, aerospace, and insulators to serve as innovation and pioneering for the advancement of science and technology.