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Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com 
ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
www.ijera.com 42 | P a g e 
A Study on Mechanical Properties of Vinylester Based Bio- Composite Material with Starch as a Filler Material Mr. Vignesh M*, Dr. H. G. Hanumantharaju**, Mr. Avinash S*** * (Student, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) ** (Faculty, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) *** (Student, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) ABSTRACT In composites a conglomeration produces material properties which are unavailable from individual constituent materials. The use of petroleum based products as constituents in polymer matrix composite has raised concerns regarding environmental issue and non-renewability of the resource. Therefore in this work an attempt has been made to develop a biocomposite material using untreated dupion silk fiber as reinforcement material and vinyl ester as matrix material with Potato Starch used as filler material by hand layup technique. The biocomposites were prepared in varying percentage of filler addition (0%, 10%, 20%, and 30%) and different mechanical tests (tensile, flexure and hardness) were conducted on the samples prepared to the ASTM standards. From the results of the experiments conducted on the specimen it can be concluded that the performance of 10% Starch filler content Biocomposite is satisfactory in all aspects compared to 0%, 20%, and 30% Starch filler content Biocomposites. 
Keywords - Implantation, Biocomposite, Dupion Silk Fiber, Potato Starch 
I. INTRODUCTION 
Engineering Materials are used in medical application to make devices to replace a part or a function of the body. Large numbers of polymeric materials alone and in combination with other materials are becoming increasingly significant in the field of biomaterials. But the use of petroleum based products as constituents in polymer matrix composite has raised concerns regarding environmental issue and non- renewability of the resource. Hence the problems associated with it have initiated the efforts to develop Biocomposites. The biocomposite have one or more constituents that are obtained from natural renewable resources also they may have partial or complete degradation and they do not emit any toxic substance during production and disposal process. By successfully producing biocomposite, we may be able to substitute the conventional petroleum-based plastics in various applications. Metals and bioceramics for biomedical application have yielded limited successes yet substantial mismatch between their properties and bone tissue persist, thereby punctuating the need for tissue engineered products. However, metals commonly induce stress shielding and will eventually experience wear debris, ultimately leading to implant failure [1]. For example, a fractured bone, fixated with a rigid, non-biodegradable stainless steel implant, has a tendency for re-fracture upon removal of the implant. The bone does not carry sufficient 
load during the healing process, because the load is carried by the rigid stainless steel [2]. However an implant prepared from biodegradable polymer can be engineered to degrade at a rate that will slowly transfer load to the healing bone [3] as shown in Graph 1. Materials used to achieve bone regeneration are diverse but not limited to metals, ceramics, synthetic polymers, naturally derived polymers, and other biocompatible substances. Success has been found by combining these materials as a strategy to eliminate the disadvantages of an individual material. In the case of materials where starch is used as an additive to a conventional plastic matrix, the polymer in contact with the soil and/or water is attacked by the microbes. The microbes digest the starch, leaving behind a porous, sponge like structure with a high interfacial area, and low structural strength (refer graph 1). When the starch component has been depleted, the polymer matrix begins to be degraded by an enzymatic attack. Each reaction results in the scission of a molecule, slowly reducing the weight of the matrix until the entire material has been digested [4]. 
RESEARCH ARTICLE OPEN ACCESS
Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com 
ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
www.ijera.com 43 | P a g e 
Graph 1: Mechanical Strength vs Time for Bone and Plate The current work is an effort to utilize the natural renewable resources to develop biocomposite material for biomedical applications such as bone Plates, bone screws material for both internal, external fixations. The dupion silk fiber is a natural fiber, it is used as reinforcement in vinyl ester resin matrix and starch is used as fillers. 
II. PREPARATION OF BIOCOMPOSITES 
2.1. MATERIALS 
Unsaturated vinylester resin was selected as matrix material, Dupion silk fibers as reinforcement and Potato Starch as filler material. Vinyl ester resins having density 1.05 g/cm3 are becoming increasingly important for fibre reinforced composites. They combine the excellent mechanical, chemical and solvent resistance properties of epoxy resins with the properties found in the unsaturated polyester resins. The chemical structure of vinylester resin is shown in Fig.1 
Figure 1: chemical structure of a typical vinylester resin Silk Dupioni is a type of silk fiber created with the threads from two different silk worms. When two worms spin their cocoons close together, the fibers get tangled up; these naturally tangled fibers are then used together to make the silk thread. In spite of its delicate appearance, silk is relatively robust; the thread is rougher than regular silk as shown in Fig.2. 
Starch is the major carbohydrate reserve in plants, and represents one of the main sources of energy to sustain life. Bread, potato, rice and pasta are examples of the importance of starch in our society. Starch has also been extremely important for centuries in numerous non-food applications, for example, as glue for paper and wood, and as gum for the textile industry. Starch-based biodegradable polymers have been widely investigated in bone tissue engineering. They have good Biocompatibility, Biodegradable and its degradation products are non- toxic. Table 1: material procurement table 
Sl. No. 
MATERIALS 
SUPPLIERS 
1 
Unsaturated Vinylester Resin 
Naphtha Resins & Chemicals (p), Bangalore, India 
2 
Cobalt napthalate accelerator 
3 
Methyl Ethyl Ketone peroxide catalyst 
4 
Dupion Silk Fiber 
Silk Exchange Office, Bangalore, India 
5 
Potato Starch 
Polysales, Avenue Road Cross, Bangalore, India 
2.2. TECHNIQUE 
The laminates were prepared by the hand lay-up technique using the rectangular box. The rectangular box of dimension 19cm×12cm is cleaned with soft brush. A layer of wax is coated on the cleaned surface for the easy removal of the laminate after curing. Weighed quantity of Potato Starch (fillers), Methyl ethyl ketone peroxide (catalyst), Cobalt napthalate (accelerator) are added to Vinyl ester resin taken in the bowl and stirred well for uniform distribution. The weight of constituents to be taken for each specimen is shown in Table 2 and Table 3. The catalyst and accelerator is taken at 1ml each for the 100 g of vinyl ester resin taken. The first layer of Vinyl ester resin mixture is coated on the wax, later Dupion silk fibers shown in fig. 2 are placed in the mould and the resin mixture is poured and distributed uniformly. Same procedure is repeated until the desired thickness is obtained. Alternate layers of resin and Dupion silk fiber are placed. 
Figure 2: raw dupion silk fibers 
The laminate is cured under light pressure for 2 hrs, followed by curing at room temperature for 24 hours. By following the same procedure as said above bio-composite material having filler
Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com 
ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
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composition of 0%, 10%, 20% and 30% is prepared. Fig.3 shows the final laminate. 
Figure 3: prepared biocomposite laminate The prepared Bio-Composite materials are cut into standard ASTM Dimensions using abrasive water jet machining. 
2.3. SAMPLE PREPARATION CALCULATION 
 Density of vinyl ester resin = 1.05 g/cm3 
 Density of potato starch = 1.43 g/cm3 
 Density of silk fiber = 1.33 g/cm3 
 Volume of the mold, V = 190 x 120 x 3.5 = 79800 mm3 = 79.8 cm3 = 80 cm3 
Table 2: Composition of Biocomposite 
Samples 
% of Resin 
% of Fiber 
% of Fillers 
A 
90 
10 
0 
B 
80 
10 
10 
C 
70 
10 
20 
D 
60 
10 
30 
Table 3: Density Calculation of Samples 
Mass of Resin (grams) 
Mass of Fiber (grams) 
Mass of fillers (grams) 
Total mass (grams) 
Density (g/cm3) 
75.6 
10.64 
0 
86.24 
1.078 
67.2 
10.64 
11.44 
89.28 
1.116 
58.8 
10.64 
22.88 
92.32 
1.154 
50.4 
10.64 
34.32 
95.36 
1.192 
III. EXPERIMENTATION 
Mechanical tests such as tensile test, flexural test and hardness tests were conducted on the specimens prepared as per the ASTM standards. The tensile test and flexural test was conducted using J J Lloyd universal testing machine and the hardness test was conducted using Rockwell hardness testing machine. All the tests were carried out at room temperature. 
Figure 4: J J Lloyd UTM 
3.1. TENSILE TEST 
Tensile tests on composite specimens were carried out according to ASTM–D 638 standard to determine tensile strength and to observe the behavior of biocomposites under load. 
Figure 5: standard tensile specimen dimensions 
3.2. FLEXURAL TEST 
Flexural tests on composite specimens were carried out according to ASTM D-790 standard. 
Figure 6: standard flexural specimen dimensions 
3.3. ROCKWELL HARDNESS TEST 
The Rockwell hardness is determined by the depth of the indentation in the test material resulting from application of a given force on a specific indenter. 
IV. RESULT AND DISCUSSION 
In this section the results obtained from tension, Flexural and Hardness tests are tabulated and represented graphically to analyze the behavior of Biocomposites. 
4.1. TENSILE TEST 
The peak load and tensile strength obtained from tensile test conducted on the prepared specimens is tabulated in Table 4.
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ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
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Table 4: Tensile Strength readings of each trail 
SAMPLE 
TRIALS 
PEAK LOAD (N) 
TENSILE STRENGTH (N/mm2) 
A 
TRIAL 1 
313 
13.55 
TRIAL 2 
432 
17.36 
B 
TRIAL 1 
809 
33.72 
TRIAL 2 
882 
37.70 
C 
TRIAL 1 
792 
37.70 
TRIAL 2 
669 
28.60 
D 
TRIAL 1 
658 
26.12 
TRIAL 2 
451 
18.33 
The prepared tensile test specimens before and after the tensile test experiment is shown in the Fig.7 
Figure 7: tensile specimen before and after test 
4.1.1. EFFECT OF PEAK LOAD 
From Graph 2 it can be observed that at all filler content the highest Peak Load is for 10% filler content bio-composite with a value of 845.5 N. 
Graph 2: peak load vs starch filler 
4.1.2. EFFECT OF ULTIMATE TENSILE STRENGTH 
From Graph 3 it can be observed that at all filler content the highest Ultimate Tensile Strength is for 10% filler content bio-composite with a value of 35.71 Mpa. 
Graph 3: tensile strength vs starch filler 
4.2. FLEXURAL TEST 
The peak load and flexural strength obtained from flexural test conducted on the prepared specimens is tabulated in table 5. Table 5: flexural strength readings of each trail 
SAMPLE 
TRIALS 
PEAK LOAD (N) 
FLEXURAL STRENGTH (N/mm2) 
A 
TRIAL 1 
222 
37.82 
TRIAL 2 
217 
35.13 
B 
TRIAL 1 
102 
19.77 
TRIAL 2 
93 
18.37 
C 
TRIAL 1 
141 
30.94 
TRIAL 2 
71 
12.67 
D 
TRIAL 1 
107 
17.39 
TRIAL 2 
108 
17.60 
The prepared flexural test specimens before and after the flexural test experiment is shown in the fig.8 
Figure 8: flexural specimen before and after test 
4.2.1. EFFECT OF PEAK LOAD 
From Graph 4 it can be observed that at all filler content the highest Peak load is for 0% filler content bio-composite with a value of 219.5N. For other combinations the value of peak load is almost the same. 
0 
200 
400 
600 
800 
1000 
0 
10 
20 
30 
40 
PEAK LOAD (N) 
STARCH FILLER % 
PEAK LOAD VS STARCH FILLER % 
0 
10 
20 
30 
40 
0 
10 
20 
30 
40 
TENSILE STRENGTH (N/MM2) 
STARCH FILLER % 
TENSILE STRENGTH VS STARCH FILLER %
Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com 
ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
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Graph 4: peak load vs starch filler 
4.2.2. EFFECT OF FLEXURAL STRENGTH 
From Graph 5 it can be observed that at all filler content the highest Flexural Strength is for 0% filler content bio-composite with a value of 36.475 Mpa. 
Graph 5: Flexural Strength vs Starch Filler 
4.3. HARDNESS TEST 
Hardness is a surface property and is a measure of wear resistance on the surface of the composite. From Graph 6 it can be observed that the hardness value reduces from 0% filler content up to 20% and then increases from that point. The measured hardness number test results are shown in Table 6. 
Graph 6: HRBN vs starch filler 
Table 6: measured hardness number 
SPECIMEN 
COMPOSITION 
HRBN 
A 
Vinylester resin + Dupion silk fiber 
22.5 
B 
Vinylester resin + Dupion silk fiber + 10% Starch 
20.5 
C 
Vinylester resin + Dupion silk fiber + 20% Starch 
19.5 
D 
Vinylester resin + Dupion silk fiber + 30% Starch 
25 
4.4. MORPHOLOGICAL CHARACTERISTICS 
Below figures show the micrograph of sample revealing the morphology of Potato Starch Granules and silk fiber reinforcement. 
Figure 9: Potato Starch Granules & Silk fibers at 1000 magnification 
Figure 10: SEM micrograph of untreated Dupion silk fiber The Micrographs reveal that the bonding between reinforcement and matrix is poor and the starch granules are attracted towards the fibers since both are hydrophilic in nature. 
V. CONCLUSION 
 Bio-composites can supplement and eventually replace petroleum based composite materials in several applications thus offering new agricultural, environmental, manufacturing and consumer benefits. 
 MECHANICAL TEST 
o Tensile test - For all the Bio-composites tested, it is observed that the Peak Load and tensile strength increases up to 10% filler 
0 
50 
100 
150 
200 
250 
0 
10 
20 
30 
40 
PEAK LOAD (N) 
STARCH FILLER % 
PEAK LOAD VS STARCH FILLER % 
0 
5 
10 
15 
20 
25 
30 
35 
40 
0 
10 
20 
30 
40 
FLEXURAL STRENGTH (Mpa) 
STARCH FILLER % 
FLEXURAL STRENGTH VS STARCH FILLER % 
0 
5 
10 
15 
20 
25 
30 
0 
10 
20 
30 
40 
HRBN 
STARCH FILLER % 
HRBN VS STARCH FILLER %
Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com 
ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 
www.ijera.com 47 | P a g e 
content then it starts to reduce from that point for higher filler percentage. Hence 10% filler content has better tensile properties compared to the 0%, 20%, 30% filler content. 
o Flexural test - the flexural strength is highest for 0% filler content, it reduces and remains almost constant for 10%, 20%, and 30%. 
o Rockwell Hardness test - The hardness test results shows that 30% filler content Biocomposites has better Hardness number. 
 Therefore from the results of experiments it can be concluded that the performance of 10% filler content Biocomposites is satisfactory in all aspects compared to all other combination. 
REFERENCES 
[1] H.E. Davis and J.K. Leach, Hybrid and Composite Biomaterials in Tissue Engineering, Topics in Multifunctional Biomaterials and Devices, Ed. N Ashammakhi © 2008. 
[2] Sangamesh Kumbar, Cato Laurencin, Meng Deng, natural and synthetic biomedical polymers (Elsevier Inc.) 
[3] John C. Middleton, Arthur J. Tipton, Synthetic biodegradable polymers as orthopedic devices, Biomaterials 21 (2000) 2335-2346 
[4] A. Ashwin Kumar , Karthick. K, and K. P. Arumugam, Biodegradable Polymers and Its Applications, International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 1, No. 3, September 2011 
[5] Dr.Shivappa, Ananda.G.K, Shivakumar.N, “Mechanical Characterization of Rice Husk Flour Reinforced Vinylester Polymer Composite", International Journal of Innovative Research in Science, Engineering and Technology, ISSN: 2319-8753, Vol. 2, Issue 11, November 2013. 
[6] M.SAKTHIVEl, S.RAMESH, "Mechanical Properties of Natural Fibre (Banana, Coir, Sisal) Polymer Composites", SCIENCE PARK ISSN: 2321 – 8045, Vol-1, Issue-1, July 2013 
[7] BIRSAN, I[ulian] G[abriel]; ROMAN, I[gor]; BRIA, V[asile]; UNGUREANU, V[ictor] & CIRCIUMARU, A[drian], "STARCH - EPOXY COMPOSITES", Annals of DAAAM for 2011 & Proceedings of the 22nd International DAAAM Symposium, Volume 22, No. 1, ISSN 1726- 9679 ISBN 978-3-901509-83-4, 2011. 
[8] Shinji Ochi, "Tensile Properties of Bamboo Fiber Reinforced Biodegradable Plastics”, 
International Journal of Composite Materials, 2012, 1-4. 
[9] Munikenche Gowda T., Naidu A. C. B., and Rajput Chayya, “Some Mechanical Properties of Untreated Jute Fabric- Reinforced Polyester Composites”, Journal of Composites Part A: Applied Science and Manufacturing, vol.30, pp. 277- 284, 1999. 
[10] Manikandan Nair K.C., Diwan S. M., Thomas S., “Tensile properties of short sisal fibre reinforced polystyrene composites” Journal of Applied Polymer Science, New York, vol.60, pp.1483-1497, 1996. 
[11] Paramasivam T., Abdulkalam A. P. J., “On the study of natural fibre composites”. Fibre Science and Technology, New Delhi, vol.1, pp.85-98, 1974. 
[12] Shah A. N. and Lakkad S. C., “Mechanical Properties Of Jute-Reinforced Plastics”, Fibre Science and Technology vol.15 pp.41- 46, 1981. 
[13] Pickering K.L., Li Y., Farrell R.L., & Lay M., “Interfacial modification of hemp fibre reinforced composites using fungal and alkali treatment”. Biobased Material and Bioenergy, vol.1 (1), pp.109-117, 2007. 
[14] Gassan J. and Bledzki A.K., “The influence of fiber-surface treatment on the mechanical properties of jute-polypropylene composites”. Composites Part-A vol.28, pp.1001-1005, 1997. 
[15] K. Murali Mohan Rao, K. Mohana Rao, "Extraction and tensile properties of natural fibers: Vakka, date and bamboo Composite Structures" 77 (2007) 288–295.

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A Study on Mechanical Properties of Vinylester Based BioComposite Material with Starch as a Filler Material

  • 1. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 42 | P a g e A Study on Mechanical Properties of Vinylester Based Bio- Composite Material with Starch as a Filler Material Mr. Vignesh M*, Dr. H. G. Hanumantharaju**, Mr. Avinash S*** * (Student, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) ** (Faculty, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) *** (Student, dept. of Mechanical Engineering, UVCE, Bangalore, Karnataka, India) ABSTRACT In composites a conglomeration produces material properties which are unavailable from individual constituent materials. The use of petroleum based products as constituents in polymer matrix composite has raised concerns regarding environmental issue and non-renewability of the resource. Therefore in this work an attempt has been made to develop a biocomposite material using untreated dupion silk fiber as reinforcement material and vinyl ester as matrix material with Potato Starch used as filler material by hand layup technique. The biocomposites were prepared in varying percentage of filler addition (0%, 10%, 20%, and 30%) and different mechanical tests (tensile, flexure and hardness) were conducted on the samples prepared to the ASTM standards. From the results of the experiments conducted on the specimen it can be concluded that the performance of 10% Starch filler content Biocomposite is satisfactory in all aspects compared to 0%, 20%, and 30% Starch filler content Biocomposites. Keywords - Implantation, Biocomposite, Dupion Silk Fiber, Potato Starch I. INTRODUCTION Engineering Materials are used in medical application to make devices to replace a part or a function of the body. Large numbers of polymeric materials alone and in combination with other materials are becoming increasingly significant in the field of biomaterials. But the use of petroleum based products as constituents in polymer matrix composite has raised concerns regarding environmental issue and non- renewability of the resource. Hence the problems associated with it have initiated the efforts to develop Biocomposites. The biocomposite have one or more constituents that are obtained from natural renewable resources also they may have partial or complete degradation and they do not emit any toxic substance during production and disposal process. By successfully producing biocomposite, we may be able to substitute the conventional petroleum-based plastics in various applications. Metals and bioceramics for biomedical application have yielded limited successes yet substantial mismatch between their properties and bone tissue persist, thereby punctuating the need for tissue engineered products. However, metals commonly induce stress shielding and will eventually experience wear debris, ultimately leading to implant failure [1]. For example, a fractured bone, fixated with a rigid, non-biodegradable stainless steel implant, has a tendency for re-fracture upon removal of the implant. The bone does not carry sufficient load during the healing process, because the load is carried by the rigid stainless steel [2]. However an implant prepared from biodegradable polymer can be engineered to degrade at a rate that will slowly transfer load to the healing bone [3] as shown in Graph 1. Materials used to achieve bone regeneration are diverse but not limited to metals, ceramics, synthetic polymers, naturally derived polymers, and other biocompatible substances. Success has been found by combining these materials as a strategy to eliminate the disadvantages of an individual material. In the case of materials where starch is used as an additive to a conventional plastic matrix, the polymer in contact with the soil and/or water is attacked by the microbes. The microbes digest the starch, leaving behind a porous, sponge like structure with a high interfacial area, and low structural strength (refer graph 1). When the starch component has been depleted, the polymer matrix begins to be degraded by an enzymatic attack. Each reaction results in the scission of a molecule, slowly reducing the weight of the matrix until the entire material has been digested [4]. RESEARCH ARTICLE OPEN ACCESS
  • 2. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 43 | P a g e Graph 1: Mechanical Strength vs Time for Bone and Plate The current work is an effort to utilize the natural renewable resources to develop biocomposite material for biomedical applications such as bone Plates, bone screws material for both internal, external fixations. The dupion silk fiber is a natural fiber, it is used as reinforcement in vinyl ester resin matrix and starch is used as fillers. II. PREPARATION OF BIOCOMPOSITES 2.1. MATERIALS Unsaturated vinylester resin was selected as matrix material, Dupion silk fibers as reinforcement and Potato Starch as filler material. Vinyl ester resins having density 1.05 g/cm3 are becoming increasingly important for fibre reinforced composites. They combine the excellent mechanical, chemical and solvent resistance properties of epoxy resins with the properties found in the unsaturated polyester resins. The chemical structure of vinylester resin is shown in Fig.1 Figure 1: chemical structure of a typical vinylester resin Silk Dupioni is a type of silk fiber created with the threads from two different silk worms. When two worms spin their cocoons close together, the fibers get tangled up; these naturally tangled fibers are then used together to make the silk thread. In spite of its delicate appearance, silk is relatively robust; the thread is rougher than regular silk as shown in Fig.2. Starch is the major carbohydrate reserve in plants, and represents one of the main sources of energy to sustain life. Bread, potato, rice and pasta are examples of the importance of starch in our society. Starch has also been extremely important for centuries in numerous non-food applications, for example, as glue for paper and wood, and as gum for the textile industry. Starch-based biodegradable polymers have been widely investigated in bone tissue engineering. They have good Biocompatibility, Biodegradable and its degradation products are non- toxic. Table 1: material procurement table Sl. No. MATERIALS SUPPLIERS 1 Unsaturated Vinylester Resin Naphtha Resins & Chemicals (p), Bangalore, India 2 Cobalt napthalate accelerator 3 Methyl Ethyl Ketone peroxide catalyst 4 Dupion Silk Fiber Silk Exchange Office, Bangalore, India 5 Potato Starch Polysales, Avenue Road Cross, Bangalore, India 2.2. TECHNIQUE The laminates were prepared by the hand lay-up technique using the rectangular box. The rectangular box of dimension 19cm×12cm is cleaned with soft brush. A layer of wax is coated on the cleaned surface for the easy removal of the laminate after curing. Weighed quantity of Potato Starch (fillers), Methyl ethyl ketone peroxide (catalyst), Cobalt napthalate (accelerator) are added to Vinyl ester resin taken in the bowl and stirred well for uniform distribution. The weight of constituents to be taken for each specimen is shown in Table 2 and Table 3. The catalyst and accelerator is taken at 1ml each for the 100 g of vinyl ester resin taken. The first layer of Vinyl ester resin mixture is coated on the wax, later Dupion silk fibers shown in fig. 2 are placed in the mould and the resin mixture is poured and distributed uniformly. Same procedure is repeated until the desired thickness is obtained. Alternate layers of resin and Dupion silk fiber are placed. Figure 2: raw dupion silk fibers The laminate is cured under light pressure for 2 hrs, followed by curing at room temperature for 24 hours. By following the same procedure as said above bio-composite material having filler
  • 3. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 44 | P a g e composition of 0%, 10%, 20% and 30% is prepared. Fig.3 shows the final laminate. Figure 3: prepared biocomposite laminate The prepared Bio-Composite materials are cut into standard ASTM Dimensions using abrasive water jet machining. 2.3. SAMPLE PREPARATION CALCULATION  Density of vinyl ester resin = 1.05 g/cm3  Density of potato starch = 1.43 g/cm3  Density of silk fiber = 1.33 g/cm3  Volume of the mold, V = 190 x 120 x 3.5 = 79800 mm3 = 79.8 cm3 = 80 cm3 Table 2: Composition of Biocomposite Samples % of Resin % of Fiber % of Fillers A 90 10 0 B 80 10 10 C 70 10 20 D 60 10 30 Table 3: Density Calculation of Samples Mass of Resin (grams) Mass of Fiber (grams) Mass of fillers (grams) Total mass (grams) Density (g/cm3) 75.6 10.64 0 86.24 1.078 67.2 10.64 11.44 89.28 1.116 58.8 10.64 22.88 92.32 1.154 50.4 10.64 34.32 95.36 1.192 III. EXPERIMENTATION Mechanical tests such as tensile test, flexural test and hardness tests were conducted on the specimens prepared as per the ASTM standards. The tensile test and flexural test was conducted using J J Lloyd universal testing machine and the hardness test was conducted using Rockwell hardness testing machine. All the tests were carried out at room temperature. Figure 4: J J Lloyd UTM 3.1. TENSILE TEST Tensile tests on composite specimens were carried out according to ASTM–D 638 standard to determine tensile strength and to observe the behavior of biocomposites under load. Figure 5: standard tensile specimen dimensions 3.2. FLEXURAL TEST Flexural tests on composite specimens were carried out according to ASTM D-790 standard. Figure 6: standard flexural specimen dimensions 3.3. ROCKWELL HARDNESS TEST The Rockwell hardness is determined by the depth of the indentation in the test material resulting from application of a given force on a specific indenter. IV. RESULT AND DISCUSSION In this section the results obtained from tension, Flexural and Hardness tests are tabulated and represented graphically to analyze the behavior of Biocomposites. 4.1. TENSILE TEST The peak load and tensile strength obtained from tensile test conducted on the prepared specimens is tabulated in Table 4.
  • 4. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 45 | P a g e Table 4: Tensile Strength readings of each trail SAMPLE TRIALS PEAK LOAD (N) TENSILE STRENGTH (N/mm2) A TRIAL 1 313 13.55 TRIAL 2 432 17.36 B TRIAL 1 809 33.72 TRIAL 2 882 37.70 C TRIAL 1 792 37.70 TRIAL 2 669 28.60 D TRIAL 1 658 26.12 TRIAL 2 451 18.33 The prepared tensile test specimens before and after the tensile test experiment is shown in the Fig.7 Figure 7: tensile specimen before and after test 4.1.1. EFFECT OF PEAK LOAD From Graph 2 it can be observed that at all filler content the highest Peak Load is for 10% filler content bio-composite with a value of 845.5 N. Graph 2: peak load vs starch filler 4.1.2. EFFECT OF ULTIMATE TENSILE STRENGTH From Graph 3 it can be observed that at all filler content the highest Ultimate Tensile Strength is for 10% filler content bio-composite with a value of 35.71 Mpa. Graph 3: tensile strength vs starch filler 4.2. FLEXURAL TEST The peak load and flexural strength obtained from flexural test conducted on the prepared specimens is tabulated in table 5. Table 5: flexural strength readings of each trail SAMPLE TRIALS PEAK LOAD (N) FLEXURAL STRENGTH (N/mm2) A TRIAL 1 222 37.82 TRIAL 2 217 35.13 B TRIAL 1 102 19.77 TRIAL 2 93 18.37 C TRIAL 1 141 30.94 TRIAL 2 71 12.67 D TRIAL 1 107 17.39 TRIAL 2 108 17.60 The prepared flexural test specimens before and after the flexural test experiment is shown in the fig.8 Figure 8: flexural specimen before and after test 4.2.1. EFFECT OF PEAK LOAD From Graph 4 it can be observed that at all filler content the highest Peak load is for 0% filler content bio-composite with a value of 219.5N. For other combinations the value of peak load is almost the same. 0 200 400 600 800 1000 0 10 20 30 40 PEAK LOAD (N) STARCH FILLER % PEAK LOAD VS STARCH FILLER % 0 10 20 30 40 0 10 20 30 40 TENSILE STRENGTH (N/MM2) STARCH FILLER % TENSILE STRENGTH VS STARCH FILLER %
  • 5. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 46 | P a g e Graph 4: peak load vs starch filler 4.2.2. EFFECT OF FLEXURAL STRENGTH From Graph 5 it can be observed that at all filler content the highest Flexural Strength is for 0% filler content bio-composite with a value of 36.475 Mpa. Graph 5: Flexural Strength vs Starch Filler 4.3. HARDNESS TEST Hardness is a surface property and is a measure of wear resistance on the surface of the composite. From Graph 6 it can be observed that the hardness value reduces from 0% filler content up to 20% and then increases from that point. The measured hardness number test results are shown in Table 6. Graph 6: HRBN vs starch filler Table 6: measured hardness number SPECIMEN COMPOSITION HRBN A Vinylester resin + Dupion silk fiber 22.5 B Vinylester resin + Dupion silk fiber + 10% Starch 20.5 C Vinylester resin + Dupion silk fiber + 20% Starch 19.5 D Vinylester resin + Dupion silk fiber + 30% Starch 25 4.4. MORPHOLOGICAL CHARACTERISTICS Below figures show the micrograph of sample revealing the morphology of Potato Starch Granules and silk fiber reinforcement. Figure 9: Potato Starch Granules & Silk fibers at 1000 magnification Figure 10: SEM micrograph of untreated Dupion silk fiber The Micrographs reveal that the bonding between reinforcement and matrix is poor and the starch granules are attracted towards the fibers since both are hydrophilic in nature. V. CONCLUSION  Bio-composites can supplement and eventually replace petroleum based composite materials in several applications thus offering new agricultural, environmental, manufacturing and consumer benefits.  MECHANICAL TEST o Tensile test - For all the Bio-composites tested, it is observed that the Peak Load and tensile strength increases up to 10% filler 0 50 100 150 200 250 0 10 20 30 40 PEAK LOAD (N) STARCH FILLER % PEAK LOAD VS STARCH FILLER % 0 5 10 15 20 25 30 35 40 0 10 20 30 40 FLEXURAL STRENGTH (Mpa) STARCH FILLER % FLEXURAL STRENGTH VS STARCH FILLER % 0 5 10 15 20 25 30 0 10 20 30 40 HRBN STARCH FILLER % HRBN VS STARCH FILLER %
  • 6. Mr. Vignesh M et al Int. Journal of Engineering Research and Applications www.ijera.com ISSN : 2248-9622, Vol. 4, Issue 11( Version 1), November 2014, pp.42-47 www.ijera.com 47 | P a g e content then it starts to reduce from that point for higher filler percentage. Hence 10% filler content has better tensile properties compared to the 0%, 20%, 30% filler content. o Flexural test - the flexural strength is highest for 0% filler content, it reduces and remains almost constant for 10%, 20%, and 30%. o Rockwell Hardness test - The hardness test results shows that 30% filler content Biocomposites has better Hardness number.  Therefore from the results of experiments it can be concluded that the performance of 10% filler content Biocomposites is satisfactory in all aspects compared to all other combination. REFERENCES [1] H.E. Davis and J.K. Leach, Hybrid and Composite Biomaterials in Tissue Engineering, Topics in Multifunctional Biomaterials and Devices, Ed. N Ashammakhi © 2008. [2] Sangamesh Kumbar, Cato Laurencin, Meng Deng, natural and synthetic biomedical polymers (Elsevier Inc.) [3] John C. Middleton, Arthur J. Tipton, Synthetic biodegradable polymers as orthopedic devices, Biomaterials 21 (2000) 2335-2346 [4] A. Ashwin Kumar , Karthick. K, and K. P. Arumugam, Biodegradable Polymers and Its Applications, International Journal of Bioscience, Biochemistry and Bioinformatics, Vol. 1, No. 3, September 2011 [5] Dr.Shivappa, Ananda.G.K, Shivakumar.N, “Mechanical Characterization of Rice Husk Flour Reinforced Vinylester Polymer Composite", International Journal of Innovative Research in Science, Engineering and Technology, ISSN: 2319-8753, Vol. 2, Issue 11, November 2013. [6] M.SAKTHIVEl, S.RAMESH, "Mechanical Properties of Natural Fibre (Banana, Coir, Sisal) Polymer Composites", SCIENCE PARK ISSN: 2321 – 8045, Vol-1, Issue-1, July 2013 [7] BIRSAN, I[ulian] G[abriel]; ROMAN, I[gor]; BRIA, V[asile]; UNGUREANU, V[ictor] & CIRCIUMARU, A[drian], "STARCH - EPOXY COMPOSITES", Annals of DAAAM for 2011 & Proceedings of the 22nd International DAAAM Symposium, Volume 22, No. 1, ISSN 1726- 9679 ISBN 978-3-901509-83-4, 2011. [8] Shinji Ochi, "Tensile Properties of Bamboo Fiber Reinforced Biodegradable Plastics”, International Journal of Composite Materials, 2012, 1-4. [9] Munikenche Gowda T., Naidu A. C. B., and Rajput Chayya, “Some Mechanical Properties of Untreated Jute Fabric- Reinforced Polyester Composites”, Journal of Composites Part A: Applied Science and Manufacturing, vol.30, pp. 277- 284, 1999. [10] Manikandan Nair K.C., Diwan S. M., Thomas S., “Tensile properties of short sisal fibre reinforced polystyrene composites” Journal of Applied Polymer Science, New York, vol.60, pp.1483-1497, 1996. [11] Paramasivam T., Abdulkalam A. P. J., “On the study of natural fibre composites”. Fibre Science and Technology, New Delhi, vol.1, pp.85-98, 1974. [12] Shah A. N. and Lakkad S. C., “Mechanical Properties Of Jute-Reinforced Plastics”, Fibre Science and Technology vol.15 pp.41- 46, 1981. [13] Pickering K.L., Li Y., Farrell R.L., & Lay M., “Interfacial modification of hemp fibre reinforced composites using fungal and alkali treatment”. Biobased Material and Bioenergy, vol.1 (1), pp.109-117, 2007. [14] Gassan J. and Bledzki A.K., “The influence of fiber-surface treatment on the mechanical properties of jute-polypropylene composites”. Composites Part-A vol.28, pp.1001-1005, 1997. [15] K. Murali Mohan Rao, K. Mohana Rao, "Extraction and tensile properties of natural fibers: Vakka, date and bamboo Composite Structures" 77 (2007) 288–295.