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Synthesis and Characterization of Methyl Methacrylate Modified Poly (Ester-Amide) Resins from Melia Azedarach Seed Oil as Coating Material

Sageer Ahamad, S. A. Ahmad and A. Hasnat*

Natural Product and Polymer Research Laboratory, Department of Chemistry, G.F. College (M.J.P. Rohilkhand University) Shahjahanpur, U.P. 242001, India

DOI : http://dx.doi.org/10.13005/msri/130108

Article Publishing History
Article Received on : 20 Oct 2015
Article Accepted on : 11 Feb 2016
Article Published : 11 Feb 2016
Plagiarism Check: Yes
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ABSTRACT:

Synthesis of polymeric materials from natural renewable resources has attracted a lot of attention of researcher throughout the world as they not only reduce the dependency on petrochemicals but also friendly to the environment. Utilization of non-traditional and non-edible vegetable oils in the synthesis of valuable polymeric materials solves the problem of waste disposal as well as bringing down the cost of end products. Melia azedrach seed oil (MASO), a non-traditional and non-edible seed oil is utilized for the synthesis of poly(ester-amide) (MAPEA) by the aminolysis with diethanolamine followed by step-growth polymerization with phthalicacid. To improve the performances and utility of the MAPEA,methyl methacrylate (MMA) classified as hard monomer in the literature of acrylate embedded to it in different phr to obtained methyl methacrylate modified poly (ester-amide) (MMMAPEA) resins. The MMMAPEA resins were characterized by physic-chemical analysis as per standard reported methods. The structural elucidation of the resin was carried out by spectral analyses. Physico-mechanical and chemical/corrosion resistance performances of the MMMAPEA resins were investigated for the optimization of MMA content.

KEYWORDS: Melia azedarach; methylmethacrylate; Poly (ester-amide); vegetable oil; coatings

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Ahamad S, Ahmad S. A, Hasnat A. Synthesis and Characterization of Methyl Methacrylate Modified Poly (Ester-Amide) Resins from Melia Azedarach Seed Oil as Coating Material. Mat.Sci.Res.India;13(1)


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Ahamad S, Ahmad S. A, Hasnat A. Synthesis and Characterization of Methyl Methacrylate Modified Poly (Ester-Amide) Resins from Melia Azedarach Seed Oil as Coating Material. Mat.Sci.Res.India;13(1). Available from: http://www.materialsciencejournal.org/?p=3772


Introduction

Polymeric materials are playing very important role in the modern society and are replacing metals in diverse field of life.1-3 However, the major drawbacks of polymeric materials are their non-biodegradability especially those derived from petrochemicals.4,5 Furthermore use of petrochemicals largely affected the environment with the increase in emission of green house gases and accumulation of non-biodegradable waste on earth6. Worldwide potential demands for replacing petroleum derived raw materials with renewable ones are quite significant due to both realizations that our petroleum resources are finite and not suitable for environment.6,7 Recent investigations are therefore, focused on producing polymeric materials from natural renewable resources which have ability to grow again and again and also posse’s inbuilt biodegradability. 8

Among different renewable resources vegetable oils obtained from the different seeds play vital role in the synthesis of polymers.9 Seed oils are cost effective, eco-friendly, eco-toxic towards humans andare also biodegradable in nature.9-11 Common seed oils such as linseed,12 castor,9 soybean9 and sunflower13 have been largely used in the synthesis of low molecular weight polymers like alkyds, epoxies, poly(urethane)s, interpenetrating polymer networks (IPNs) poly(ester-amide)s and many others.14 These polymers are extensively used in the coatings, paints, and adhesives and bioengineering industries. Among aforesaid traditional oils some of them posses the medicinal values and edible too.15 Therefore it is desirable to explore the spectrum of nature’s blessing and utilized non-edible oils in the synthesis of valuable polymer to maintain equilibrium of demand and availability of feed stock.

Melia azedarach belongs to the family meliaceae, largely cultivated in rural areas for its valuable wood. Its seed contain about 40 % triglyceride oil with appropriate composition of unsaturated and saturated fatty acids.16 The results of pysico-chemical characterization indicate that the oil is a suitable starting material for the polymer synthesis polymer with film forming ability.

Poly (ester-amide) resin obtained from different seed oils are amide modified alkyds known for improve film characteristic over traditional alkyds in terms of hardness, water vapor resistance and durability in many service environment.17-19 However their utilization as viable coating materials is limited as they required high baking temperature for curing.20,21 Curing of the polymeric material at elevated temperature is a difficult process as well as energy consuming too.On review of literature it has been found that incorporation of metals, metalloids and organic moieties like styrene, vinyl acetate, poly (styrene-co-maleic anhydride) to the oil based polymers reduces the curing temperature as well as also enhances the scratch hardness and protective efficiency.10,22 Methyl methacrylate is classified in the literature of acrylates as a monomer of conferring the hardness to the resulting polymers.23

Keeping these facts in mind we have made an effort to develop the methylmethacrylate modified poly (ester-amide) with the objective toprovide the more practicable utility to the Melia azedarach seed oil a renewable resource of the nature generally destroyed in every season.

Experimental

Melia azedarach seed oil (MASO) was extracted from the crushed seeds of Melia azedarach collected from the different places of the shahjahanpur, U.P. India, through the soxhlet apparatus by using petroleum ether as a solvent (60-80 oC). The results of physico-chemical analyses and fatty acid profile11 of MASO is presented in Table 1. Phthalic acid, diethyl ether, methanol, xylene and methyl methacrylate were procured from Merck, India. Diethanol amine of analytical grade procured from the s.d. Fine Chemicals, India and was distilled under reduced pressure before use.

Table 1: Physico-chemical characterization of MASO

S. No.

Characteristic

MASO

1.

Oil content

40

2.

Gardener color

6

3.

Specific gravity

0.93

4.

Refractive index

1.4691

5.

Acid value (mg of KOH)

4.42

6.

Iodine value

134.7

7.

Saponification value

190.8

8.

Fatty acid composition

 

 

Saturated (Palmitic and Stearic)

11.4

 

Unsaturated (Oleic and Linoleic)

88.6

 

Syntheses

N,N-bis (2-hydroxy ethyl) Melia azedarach oil fatty amide (HEMAFA) and Melia azedarach Poly(ester-amide) (MAPEA)

HEMAFA and MAPEA were synthesized and characterize as per previously reported methods11

Methyl methacrylate modified poly (ester-amide) (MMMAPEA)

MAPEA dissolved in xylene placed in a four necked round bottom flask equipped with water condenser, nitrogen inlet tube, thermometer and mechanical stirrer. The content was heated up to 140±5oC and then methyl methacrylate (MMA) in different per hundred of resin (phr) along with bezoyl peroxide (0.1 wt% of MMA) added slowly in the aforementioned reaction mixture. The reaction mixtures were allowed continue for two hrs to obtained MMMAPEA resins as end products. On completion of reactions, the products were cooled at room temperature. The excess of solvent removed in a rotary vacuum evaporator under reduce pressure.

Characterization

Physico-chemical characterizations such as specific gravity, refractive index, viscosity, iodine value, hydroxyl value, saponification value of the developed polymers were performed as per standard reported laboratory methods.6,12 The structural elucidation of the polymer samples were done by spectral analyses. FT-IR spectrum of the MMMAPEA was recorded on FT-IR spectrophotometer (Perkin-Elmer Cetus instruments, Norwalk CT, USA) using a NaCl cell. 1H-NMR and 13C-NMR spectra were recorded on JEOL GSX 300 MHz FX-1000 spectrometer using deuterated chloroform as a solvent and tetramethylsilane (TMS) as an internal standard.

Preparation of coatings

Coatings of MMMAPEA resins were prepared on mild steel strips, 70x25x1 mm size for pysico-mechanical test and 30x10x1 mm size for chemical/corrosion resistance test. The mild steel strips were polished on various grade of silicon carbide papers, then washed with distilled water, degreased with alcohol and carbon tetrachloride. They were dried under vacuum for several hours. The coatings were developed on these specimens by brush technique using a solution of 60 wt % of resins. Coated strips were baked at 160 oC for 20 minutes. Elcometer (Model 345; Elcometer instrument, Manchester, UK) was used to measure the coating thickness. The thicknesses of these coatings were found between 75± 5µm. The coated samples were evaluated for the scratch hardness (BS 3900), bending test on conical mandrels and impact resistance (IS: 101 part 5/Sec.31988) tests. The salt spray test (ASTM b117-94) was performed in a salt mist chamber containing 3.5 wt% NaCl solutions. Chemical resistance tests of the coating samples were performed in water, acid (5 wt % HCl), alkali (5 wt% NaOH) by placing them in 3 in. diameter porcelain dishes, in aforementioned media. Periodic examinations were performed until coatings showed visual evidence of softening, deterioration in gloss, discoloration or weight loss. The results of these investigations summarized in Table 3.

Table 2: Physico-chemical characterization of HEMAFA, MAPEA and MMMAPEA

Properties

HEMAFA

MAPEA

MMMPEA-10

MMMPEA-15

MMMPEA-20

MMMPEA-25

MMMPEA-30

 

Gardener

color

6

8

7

6

6

6

6

Specific

 gravity

0.938

0.956

0.968

0.972

0.974

0.978

0.980

Inherent

viscosity

1.4697

0.612

0.626

0.636

0.648

0.652

0.656

Refractive

 index

1.4697

1.5062

1.5088

1.5098

1.5128

1.5132

1.5136

Acid

value

7.42

 

 

 

 

 

Iodine

value

65.80

36.80

32.80

31.52

30.22

29.44

27.68

 

Table 3: Physico-mechanical and chemical/corrosion resistance properties of AAMAPEA     coatings

 

 

 

 

 

Chemical/corrosion resistanceb

Resin codea

Scratch hardness (Kg)

Impact resistance (lb/in)

Bending test (1/8’)

Gloss at 45o

H2O

10 days

HCl

(5 %)

10 days

NaOH (3%) (3hrs)

NaCl

(3.5 %) 10 days

MMMAPEA-5

1.5

100

Pass

42

C

B

A

C

MMMAPEA-10

2.5

150

Pass

48

D

D

B

C

MMMAPEA-15

3.0

200

Pass

58

E

D

C

D

MMMAPEA-20

3.5

200

Pass

68

E

E

D

D

MMMAPEA-25

3.5

200

Pass

68

D

D

C

D

MMMAPEA-30

3.5

150

Fail

66

D

C

C

C

aLast digit indicates the loading of MMA in phr,

bA= film completely removed; B= film cracked and partially removed; C=loss in gloss; D=slight loss in gloss; E=unaffected

Results and Discussion

Figure 1&2 illustrate the reaction schemes for the synthesis of HEMAFA, MAPEA and MMMAPEA. The MAPEA was synthesized by the aminolysis of MASO with diethanol amine followed by the step-growth polymerization of HEMAFA with phthalic acid. MAPEA resin was then treated with methylmethacrylate in different phr (Table 2) to obtain a series of MMMAPEA resins. Methylmethacrylate was grafted at allylic position of non-conjugated fatty acid chain, free radicals serve to modify the growth of methylmethacrylate chain by chain transfer mechanism. The analytical analyses revealed that acid valuesof the reaction mixture decreases progressively during the conversion of HEMAFA to MAPEA. This is due to formation of repeating ester linkages during the condensation polymerization. On perusal of Table 2 it is reveals that, iodine value decreases gradually on increasing the MMA (phr) content but remain constant for the same amount of MAPEA in the reaction. These observations indicate that grafting occur at allylic position without affecting the unsaturation of fatty amide.

IR spectrum of MMMAPEA shows the broad bandat 3410 cm-1 for the O-H stretching vibration, band at 3080 cm-1 for Ar-H, bands at 2964 cm-1 and 2858 cm-1for CH2 asymmetric and symmetric stretching vibrations respectively. The bands for carbonyl of repeating ester linkages, ester of methacrylate and amide are appear at 1764 cm-1, 1749 cm-1 and 1652 cm-1 respectively. The characteristic bands of aromatic ring appears at 1598, 772 cm-1. 1HNMR spectrum of MMMAPEA shows the peaks at δ = 7.38-7.62 ppm due to aromatic protons of phthalic acid while proton of double bonded carbons appear at δ =5.42-5.46 ppm. CH2 attached to nitrogen of amide appear at δ 3.78-4.12 ppm where as allylic methylene and methine protons appear at 2.52 and 2.94 ppm respectively. Sharp peak for CH2 adjacent to ester appears at δ =2.14 ppm, fatty amide chain CH2 appear as multiplet at δ 1.32-1.56 ppm and proton of terminal methyl group at δ =0.96 ppm. 13 CNMR spectrum show the peaks at δ = 172.8 ppm, 170.4 ppm and δ 164.8 ppm for the carbonyls of repeating ester, ester of methacrylate and amide. Closely spaced peaks at δ 132.2-128.4 ppm due to carbon of aromatic ring.18,24 Double bonded carbons appear at132.4-126.2 ppm where as carbons of allylic methine and methylene appears at δ 54.2 and δ 46.4 ppm respectively. Peaks for chain CH2 of fatty amide appears at δ 29.8-24.6 ppm while carbon of terminal methyl group appears at 14.6 ppm.

Coating properties

The films of MMMAPEA containing different phr of MMA (Table 3) developed on the mild steel panels to investigate the physico-mechanical as well as chemical/corrosion resistance performances. Scratch hardness values were found to improve appreciably on increasing the MMA content in MAPEA up to 20phr. This isdue to increase of pendent ester groupsof MMA which provides sites for cross-linking as well as impart adhesion of polymeric resins towards the metal surface. However, beyond this loading of MMA improvement in these properties were negligible. All the coated samples show the good impact resistance and this property further improved remarkableup to the 20 phr loading of MMA, reasonably due to increase of polar groups in the MMMAPEA which impart good adhesion between the coating material and metal surface. However above than 20 phr loading of MMA in the polymeric resin no significant improvement was observed.  Furthermore, it has been observed that loading of MMA beyond 30phr coating materials loss the fluidity and become unbrushable lumpy aggregates were formed. This is due to excessive electrostatic attractions among polar groups of different polymeric chains. Gloss values of polymeric films increases on increasing the amount of MMA, which expected for acrylate based coating materials and increased density of cross linking.14,23 The polymeric films pass the bending test on 1/8 conical mandrel up to the loading of 25phr of MMA, a characteristic of vegetable oil based coating materials.Small cracks were observed in case of MMMAPEA-30 presumably due to the excessive cross-linking which makes the film brittle. Table 3 indicates that chemical resistance ability of MMMAPEA improved up to 20 phr of MMA. MMMAPEA-20 among all MMMAPEA systems shows the best performance in water, acidic solution and salt solution. On perusal of Table 3 it has been observed that chemical resistivity of the polymer film not significantly improved after 20 phr loading of MMA where as start to deteriorate on increasing the component of MMA more than 25 phr. This is reasonably due to excessive cross-linking made the film not only brittle but also a cause of shrinkage of the film at edges. Coatings of MMMAPEA show inferior performance in alkaline medium like other oil based coating materials due presence of saponifiable ester linkages.

Figure 1

Figure 1
Click on image to enlarge

 

Figure 2

Figure 2
Click on image to enlarge

 

Conclusion

From this study it can be concluded that the non-edible, non-traditional and annually renewable significantly born of nature Melia azedarachseed oil can be utilized for the synthesis of methylmethacrylatemodified poly (ester-amide) resins. The synthesized resins were characterized by physico-chemical analyses and spectral studies. Physico-mechanical performances and corrosion/chemical resistance ability of the polymeric films were also investigated. Films of MMMAPEA resins show good performances in acidic, humid and saline environments. Furthermore, MMMAPEA-20 shows the best performance among all MMMAPEA resins. Studies show that methylmethacrylate modified Poly (ester-amide) derived from MASO is a practicable material for the coatings and paints.

Acknowledgement

The authors would like to thank the authorities of G. F. College, Shahjahanpur, UP, India for providing necessary facilities for carrying out this study.

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