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Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31
www.ijera.com 27|P a g e
Green Synthesis of Calcium Oxide Nanoparticles and Its
Applications
Ashwini Anantharaman*
, Ramalakshmi S*
, and Mary George*
* (
Department of chemistry, Stella Maris College, Chennai-86)
ABSTRACT
Green synthesis of metal oxide nanoparticles is gaining considerable interest due to the use of environmentally
friendly reactants and room temperature synthesis. This is the most preferred method of preparation as it makes
use of pollution free chemicals and encourages the use of non-toxic solvents such as water and plants extracts.
The present study is proposed with an objective to synthesize CaO nanoparticles by the eco-friendly green
synthesis using environmentally benign papaya leaf extract and Green Tea extract. The obtained CaO
nanoparticles have been characterized by UV- Vis, Fourier Transform Infrared (FTIR) X-ray Diffraction (XRD),
and Scanning Electron Microscopy (SEM) studies. The antibacterial and photocatalytic activity of the calcium
oxide nanoparticles were also analysed.
Keywords: CaO nanoparticles, Green Synthesis, Green Tea Extract, Papaya Leaf extract,
I. INTRODUCTION
The use of plant extracts in the synthesis
of nanoparticles have proven to be cost effective
and opens up a wide area in non-toxic nanoparticle
synthesis. Calcium Oxide (CaO) nanoparticles have
found several applications such as in catalysis,
adsorption, water purification and also as
antibacterial agents [1-3]. CaO is of particular
interest as it is regarded as a safe material to human
beings and animals. There are many reports on
preparation of Calcium oxide nanoparticles from
chemical methods. However, only few biogenic
syntheses are being reported in literature [4-6]. In
this work, CaO nanoparticles was synthesised using
the Papaya Leaf and Green Tea extract. Then the as
prepared CaO NPs prepared were characterized
using UV-Vis spectroscopy, Fourier Transform
Infrared (FT-IR), Powder X-ray Diffraction studies
(XRD), Scanning Electron Microscopy (SEM)
techniques. The applications such as antibacterial
and photo catalytic activity for the same were
studied.
II. MATERIALS AND METHODS
Calcium nitrate, (Ca (NO3)2. 4 H2O) from
(HI Media), Sodium hydroxide pellets (Avra
synthesis Pvt. Ltd), distilled water. The plant
extracts used for synthesis of nanoparticles were
prepared using plants such as papaya leaves
collected from the botanical garden of Stella Maris
College, Chennai. Green Tea leaves was purchased
from the Nilgris super market.
2.1 Preparation of extract from Papaya leaves
Papaya extract was prepared from 100 g of
thoroughly washed papaya leaves. It was then
boiled in 200 mL of distilled water for half an hour,
filtered with Whatmann no 1 filter paper and the
resulting extract was cooled and used for synthesis
of metal oxide nanoparticles.
2.2 Preparation of extract from Green Tea
leaves
Green tea extract was prepared from 10 g
of thoroughly washed green tea leaves. It was then
boiled in 100 mL of distilled water for half an hour,
filtered with Whatmann no 1 filter paper and the
resulting extract was cooled and used as the green
tea extract solution.
2.3 Synthesis of calcium oxide nanoparticles
using plant extracts
Ten mL of calcium nitrate solution was
added to 10 mL of papaya extract. Then, the
mixture was stirred in a magnetic stirrer for about
half an hour. NaOH was added dropwise while
stirring till a white precipitate of calcium hydroxide
was obtained. The precipitate was filtered and dried
in an air oven for an hour. The content was washed
repeatedly with distilled water to remove the
basicity of the solution. Further, the calcination was
done in the muffle furnace at 500⁰C for three hours.
Similar procedure was carried out for synthesis of
calcium oxide nanoparticles using Green Tea
extract.
III. RESULTS AND DISCUSSION
3.1 UV Diffused Reflectance Spectroscopy (UV-
DRS)
The UV spectrum of CaGT and CaP
nanoparticles are shown in Fig. 3.1.The band gap
energy of the Calcium oxide nanoparticle was
calculated using the Planck’s equation. The band
gap energy of CaO is found to be 3.44 eV and
RESEARCH ARTICLE OPEN ACCESS
Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31
www.ijera.com 28|P a g e
3.48eV for CaGT and CaP nanoparticles respectively.
300 400 500 600 700 800
0.82
0.83
0.84
0.85
0.86
0.87
0.88
0.89
0.90
0.91
Absorbance
wavelength (nm)
300 400 500 600 700 800
0.82
0.83
0.84
0.85
0.86
0.87
0.88
0.89
0.90
0.91
Absorbance
wavelength (nm)
Fig. 3.1 UV (DRS) absorption spectrum of CaGT and CaP nanoparticles
3.2 Infrared Spectroscopy
The prepared calcium oxide nanoparticles
(CaGT and CaP) were characterised using Perkin
Elmer FT-IR spectrometer. The FT-IR spectra of
CaGT and CaP are shown in Fig. 3. The sharp
peak at 874cm-1
is due to the presence of Ca-O-Ca
bonding and peak at 712cm-1
is due to the presence
of Ca-O bonding which identifies the presence of
calcium oxide. Broad IR bands at 3783, 2926,
1796, 1429 cm-1
show the presence of hydroxyl
group, carboxylic group, amines and amides which
confirms that the phytoconstituents could possibly
enhance the stabilization of Calcium oxide
nanoparticles.
4000 3500 3000 2500 2000 1500 1000 500
30
40
50
60
70
80
90
100
110
%T
Wavelength (cm
-1
)
4000 3500 3000 2500 2000 1500 1000 500
40
50
60
70
80
90
100
wavelength (cm
-1
)
%T
Fig. 3.2 FT-IR spectra of CaGT and CaP nanoparticles
3.3 Powder X-Ray Diffraction studies
The XRD pattern of CaO NPs are shown in
Fig 4. The XRD pattern of CaO NPs shows good
agreement with the standard JCPDS NO. 77-2376.
The pure cubic phase of Calcium oxide was formed in
both CaGT and CaP composite. The average
crystallite size were determined by a the debye-
Scherer formula and found to be 23 nm and 24 nm for
CaGT and CaP respectively, which confirmed that the
synthesized nanocomposites are nanocrystalline in
nature.
0 10 20 30 40 50 60 70 80 90
0
1000
2000
3000
4000
5000
6000
7000
Intensity(a.u.)
2 Theta (degree)
10 20 30 40 50 60 70 80
0
20
40
60
80
100
Intensity(a.u.)
2 theata (degree)
Fig. 3.3 XRD pattern of CaGT and CaP nanoparticles
Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31
www.ijera.com 29|P a g e
3.4 Scanning Electron Microscopy
SEM images showed the particle size
ranging from 86-117 nm for CaGT whereas for CaP,
it ranged from 89-148 nm as shown in Fig 5. The
SEM images of CaGT and CaP indicated
agglomeration, which revealed that the synthesized
nanoparticles are porous.
Fig. 3.4 SEM images of CaGT and CaP nanoparticles
3.5 Antibacterial Studies
Antibacterial activity of the synthesized
Calcium oxide nanoparticles from Green Tea extract and
papaya extract were studied using the disc-diffusion
method.
Fig. 3.5 Antibacterial activity of CaGT on S.aureus, B.cereus, E.coli and P. aeruginosa
Fig.3. 6 Antibacterial activity of CaP on S.aureus, B.cereus, E.coli and P. aeruginosa
The synthesized calcium oxide nanoparticles
which were placed on the surface of the bacteria medium
–inoculated agar medium were measured for inhibition.
A a 50 µl concentration of calcium oxide nanoparticles,
B 100 µl concentration of calcium oxide nanoparticles,
C positive control (Green Tea extract, papaya extract)
and D negative control. The, synthesized nanoparticles
showed inhibition in both gram positive and gram
negative bacteria.
3.6 Photocatalytic Studies
The UV–Vis absorption curves of CaGT and
CaP nanoparticles showing photocatalytic studies are
represented in Fig 3.7 and Fig 3.8 respectively. The
photocatalytic activity of the synthesized calcium oxide
nanoparticles, CaGT and CaP were studied by degrading
Congo red(CR ) dye. To 100 mL of 25 ppm concentrated
Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31
www.ijera.com 30|P a g e
dye, 100 mg of the catalysts (CaGT and CaP) were added
and the degradation was carried out as mentioned above
and the results were recorded.. Initially UV absorption of
the CR dye is measured followed which the absorption is
measured periodically at an interval of 30 min for 3 hrs
with the addition of the catalyst. The Figure shows
reduction in the absorption maximum between 350 nm
and 500 nm which is a clear indication of the
photocatalytic activity of CaGT and CaP nanoparticles.
Fig 3.7 Photocatalytic degradation of Congo Red using CaGT nanoparticles
Fig 3.8 Photocatalytic degradation of Congo Red using CaP nanoparticles
3.6.1 Effect of Amount of CaGT and CaP
Catalyst on Decolourization of CR
After equilibration time of 20 minutes,
photocatalytic experiments were carried out for 3
hours. Concentration of CR at different time
intervals was determined spectrophotometrically
and the results are shown as a plot of ln(C/CO) Vs
time in Fig. 3.9 and 3.10 respectively, where C is
the concentration at various time intervals and CO
the initial concentration. A linear fit plot was
obtained which indicated that the reaction
followed the pseudo first order rate kinetics. Rate
constants were calculated from each linear plot.
Increase in the pseudo first order rate constant
with increase of CaP catalyst indicated that the
decolourization was truly photocatalytic.
Fig 3.9 Plot of ln(C/Co) Vs Time for the degradation of CR on CaGT nanoparticles
Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application
www.ijera.com
ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31
www.ijera.com 31|P a g e
Fig 3.10 Plot of ln(C/Co) Vs Time for the degradation of CR on CaP nanoparticles
3.6.2 Efficiency of the Photocatalytic behaviour
of the as prepared Catalyst
A comparison of the efficiency of the
photocatalytic behavior of CaGT and CaP were
studied. It is observed from Fig (3.11) that CaP
.has a higher photocatalytic activity when
compared to CaP. This may be due to the high
antioxidant property of papaya which is used as a
stabilizing /capping agent in the synthesis of the
catalyst. CaP prevents the recombination of
electrons from the conduction band to the valence
band thereby enhancing its photocatalytic activity
than CaGT nanoparticles.
Fig 3.11 Plot of Rate Constant against CaGT and CaP nanoparticles
IV. CONCLUSION
The proposed study was undertaken for thee
development of an economic and eco-friendly method
of synthesizing CaO nanoparticles. The antibacterial
studies of CaGT and CaP indicated that the synthesized
nanoparticles showed sensitivity to both Gram negative
and Gram positive bacteria. CaP nanoparticles showed
higher photocatalytic activity than CaGT nanoparticles.
Hence, calcium oxide nanoparticles synthesized using
papaya leaves acts as an excellent photocatalyst in for
degradation of dyes from textile industries.
REFERENCES
[1]. N.Madhusudhana, K.Yogendra and
K.Mahadevan, A comparative study on
Photocatalytic degradation of Violet
GL2B azo dye using CaO and TiO2
nanoparticles. Int J Eng Res Appl, 2(5),
2012, 1300-1307.
[2]. A.Roy, S . Samiran, M .Bhattacharya,.;
J. Bhattacharya, Antimicrobial Activity
of CaO Nanoparticles. J Biomed
Nanotechnol. 9(9), 2013,1–8.
[3]. X. B Hai, Z. S Xiao, H. L Xiao and Y. L
Sheng, Synthesis of porous CaO
microsphere and its application in
catalyzing transesterification reaction for
biodiesel. Trans. Nonferrous Met, 19(3),
2009, 674-77.
[4]. N.Madhusudhana.; K.Yogendra and K.
M Mahadevan.. Decolorization of
Coralene Dark Red 2B azo dye using
Calcium Oxide Nanoparticle as an
adsorbent. Int. J. Res. Chem. Environ.,
2(2), 2012, 21-25.
[5]. S. Priscilla Prabhavathi, Ranjith,
Shameela Rajam, Maruthamuthu and
Kingsley Raja, sol-gel methods of
synthesis of MgO and CaO nanoparticles
and their characterization. World Journal
of Pharmaceutical Research., 3(7),
2014, 362–370.
[6]. C. Bhavya and K.Yogendra. Study on
The Synthesis,“Characterization and
Photocatalytic Activity of CaO
Nanoparticle Against Some Selected
Azo Dyes, Indian Journal of Applied
Research, 5(6) 2015, 361–365.

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Green Synthesis of Calcium Oxide Nanoparticles and Its Applications

  • 1. Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31 www.ijera.com 27|P a g e Green Synthesis of Calcium Oxide Nanoparticles and Its Applications Ashwini Anantharaman* , Ramalakshmi S* , and Mary George* * ( Department of chemistry, Stella Maris College, Chennai-86) ABSTRACT Green synthesis of metal oxide nanoparticles is gaining considerable interest due to the use of environmentally friendly reactants and room temperature synthesis. This is the most preferred method of preparation as it makes use of pollution free chemicals and encourages the use of non-toxic solvents such as water and plants extracts. The present study is proposed with an objective to synthesize CaO nanoparticles by the eco-friendly green synthesis using environmentally benign papaya leaf extract and Green Tea extract. The obtained CaO nanoparticles have been characterized by UV- Vis, Fourier Transform Infrared (FTIR) X-ray Diffraction (XRD), and Scanning Electron Microscopy (SEM) studies. The antibacterial and photocatalytic activity of the calcium oxide nanoparticles were also analysed. Keywords: CaO nanoparticles, Green Synthesis, Green Tea Extract, Papaya Leaf extract, I. INTRODUCTION The use of plant extracts in the synthesis of nanoparticles have proven to be cost effective and opens up a wide area in non-toxic nanoparticle synthesis. Calcium Oxide (CaO) nanoparticles have found several applications such as in catalysis, adsorption, water purification and also as antibacterial agents [1-3]. CaO is of particular interest as it is regarded as a safe material to human beings and animals. There are many reports on preparation of Calcium oxide nanoparticles from chemical methods. However, only few biogenic syntheses are being reported in literature [4-6]. In this work, CaO nanoparticles was synthesised using the Papaya Leaf and Green Tea extract. Then the as prepared CaO NPs prepared were characterized using UV-Vis spectroscopy, Fourier Transform Infrared (FT-IR), Powder X-ray Diffraction studies (XRD), Scanning Electron Microscopy (SEM) techniques. The applications such as antibacterial and photo catalytic activity for the same were studied. II. MATERIALS AND METHODS Calcium nitrate, (Ca (NO3)2. 4 H2O) from (HI Media), Sodium hydroxide pellets (Avra synthesis Pvt. Ltd), distilled water. The plant extracts used for synthesis of nanoparticles were prepared using plants such as papaya leaves collected from the botanical garden of Stella Maris College, Chennai. Green Tea leaves was purchased from the Nilgris super market. 2.1 Preparation of extract from Papaya leaves Papaya extract was prepared from 100 g of thoroughly washed papaya leaves. It was then boiled in 200 mL of distilled water for half an hour, filtered with Whatmann no 1 filter paper and the resulting extract was cooled and used for synthesis of metal oxide nanoparticles. 2.2 Preparation of extract from Green Tea leaves Green tea extract was prepared from 10 g of thoroughly washed green tea leaves. It was then boiled in 100 mL of distilled water for half an hour, filtered with Whatmann no 1 filter paper and the resulting extract was cooled and used as the green tea extract solution. 2.3 Synthesis of calcium oxide nanoparticles using plant extracts Ten mL of calcium nitrate solution was added to 10 mL of papaya extract. Then, the mixture was stirred in a magnetic stirrer for about half an hour. NaOH was added dropwise while stirring till a white precipitate of calcium hydroxide was obtained. The precipitate was filtered and dried in an air oven for an hour. The content was washed repeatedly with distilled water to remove the basicity of the solution. Further, the calcination was done in the muffle furnace at 500⁰C for three hours. Similar procedure was carried out for synthesis of calcium oxide nanoparticles using Green Tea extract. III. RESULTS AND DISCUSSION 3.1 UV Diffused Reflectance Spectroscopy (UV- DRS) The UV spectrum of CaGT and CaP nanoparticles are shown in Fig. 3.1.The band gap energy of the Calcium oxide nanoparticle was calculated using the Planck’s equation. The band gap energy of CaO is found to be 3.44 eV and RESEARCH ARTICLE OPEN ACCESS
  • 2. Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31 www.ijera.com 28|P a g e 3.48eV for CaGT and CaP nanoparticles respectively. 300 400 500 600 700 800 0.82 0.83 0.84 0.85 0.86 0.87 0.88 0.89 0.90 0.91 Absorbance wavelength (nm) 300 400 500 600 700 800 0.82 0.83 0.84 0.85 0.86 0.87 0.88 0.89 0.90 0.91 Absorbance wavelength (nm) Fig. 3.1 UV (DRS) absorption spectrum of CaGT and CaP nanoparticles 3.2 Infrared Spectroscopy The prepared calcium oxide nanoparticles (CaGT and CaP) were characterised using Perkin Elmer FT-IR spectrometer. The FT-IR spectra of CaGT and CaP are shown in Fig. 3. The sharp peak at 874cm-1 is due to the presence of Ca-O-Ca bonding and peak at 712cm-1 is due to the presence of Ca-O bonding which identifies the presence of calcium oxide. Broad IR bands at 3783, 2926, 1796, 1429 cm-1 show the presence of hydroxyl group, carboxylic group, amines and amides which confirms that the phytoconstituents could possibly enhance the stabilization of Calcium oxide nanoparticles. 4000 3500 3000 2500 2000 1500 1000 500 30 40 50 60 70 80 90 100 110 %T Wavelength (cm -1 ) 4000 3500 3000 2500 2000 1500 1000 500 40 50 60 70 80 90 100 wavelength (cm -1 ) %T Fig. 3.2 FT-IR spectra of CaGT and CaP nanoparticles 3.3 Powder X-Ray Diffraction studies The XRD pattern of CaO NPs are shown in Fig 4. The XRD pattern of CaO NPs shows good agreement with the standard JCPDS NO. 77-2376. The pure cubic phase of Calcium oxide was formed in both CaGT and CaP composite. The average crystallite size were determined by a the debye- Scherer formula and found to be 23 nm and 24 nm for CaGT and CaP respectively, which confirmed that the synthesized nanocomposites are nanocrystalline in nature. 0 10 20 30 40 50 60 70 80 90 0 1000 2000 3000 4000 5000 6000 7000 Intensity(a.u.) 2 Theta (degree) 10 20 30 40 50 60 70 80 0 20 40 60 80 100 Intensity(a.u.) 2 theata (degree) Fig. 3.3 XRD pattern of CaGT and CaP nanoparticles
  • 3. Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31 www.ijera.com 29|P a g e 3.4 Scanning Electron Microscopy SEM images showed the particle size ranging from 86-117 nm for CaGT whereas for CaP, it ranged from 89-148 nm as shown in Fig 5. The SEM images of CaGT and CaP indicated agglomeration, which revealed that the synthesized nanoparticles are porous. Fig. 3.4 SEM images of CaGT and CaP nanoparticles 3.5 Antibacterial Studies Antibacterial activity of the synthesized Calcium oxide nanoparticles from Green Tea extract and papaya extract were studied using the disc-diffusion method. Fig. 3.5 Antibacterial activity of CaGT on S.aureus, B.cereus, E.coli and P. aeruginosa Fig.3. 6 Antibacterial activity of CaP on S.aureus, B.cereus, E.coli and P. aeruginosa The synthesized calcium oxide nanoparticles which were placed on the surface of the bacteria medium –inoculated agar medium were measured for inhibition. A a 50 µl concentration of calcium oxide nanoparticles, B 100 µl concentration of calcium oxide nanoparticles, C positive control (Green Tea extract, papaya extract) and D negative control. The, synthesized nanoparticles showed inhibition in both gram positive and gram negative bacteria. 3.6 Photocatalytic Studies The UV–Vis absorption curves of CaGT and CaP nanoparticles showing photocatalytic studies are represented in Fig 3.7 and Fig 3.8 respectively. The photocatalytic activity of the synthesized calcium oxide nanoparticles, CaGT and CaP were studied by degrading Congo red(CR ) dye. To 100 mL of 25 ppm concentrated
  • 4. Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31 www.ijera.com 30|P a g e dye, 100 mg of the catalysts (CaGT and CaP) were added and the degradation was carried out as mentioned above and the results were recorded.. Initially UV absorption of the CR dye is measured followed which the absorption is measured periodically at an interval of 30 min for 3 hrs with the addition of the catalyst. The Figure shows reduction in the absorption maximum between 350 nm and 500 nm which is a clear indication of the photocatalytic activity of CaGT and CaP nanoparticles. Fig 3.7 Photocatalytic degradation of Congo Red using CaGT nanoparticles Fig 3.8 Photocatalytic degradation of Congo Red using CaP nanoparticles 3.6.1 Effect of Amount of CaGT and CaP Catalyst on Decolourization of CR After equilibration time of 20 minutes, photocatalytic experiments were carried out for 3 hours. Concentration of CR at different time intervals was determined spectrophotometrically and the results are shown as a plot of ln(C/CO) Vs time in Fig. 3.9 and 3.10 respectively, where C is the concentration at various time intervals and CO the initial concentration. A linear fit plot was obtained which indicated that the reaction followed the pseudo first order rate kinetics. Rate constants were calculated from each linear plot. Increase in the pseudo first order rate constant with increase of CaP catalyst indicated that the decolourization was truly photocatalytic. Fig 3.9 Plot of ln(C/Co) Vs Time for the degradation of CR on CaGT nanoparticles
  • 5. Ashwini Anantharaman et al. Int. Journal of Engineering Research and Application www.ijera.com ISSN : 2248-9622, Vol. 6, Issue 10, ( Part -1) October 2016, pp.27-31 www.ijera.com 31|P a g e Fig 3.10 Plot of ln(C/Co) Vs Time for the degradation of CR on CaP nanoparticles 3.6.2 Efficiency of the Photocatalytic behaviour of the as prepared Catalyst A comparison of the efficiency of the photocatalytic behavior of CaGT and CaP were studied. It is observed from Fig (3.11) that CaP .has a higher photocatalytic activity when compared to CaP. This may be due to the high antioxidant property of papaya which is used as a stabilizing /capping agent in the synthesis of the catalyst. CaP prevents the recombination of electrons from the conduction band to the valence band thereby enhancing its photocatalytic activity than CaGT nanoparticles. Fig 3.11 Plot of Rate Constant against CaGT and CaP nanoparticles IV. CONCLUSION The proposed study was undertaken for thee development of an economic and eco-friendly method of synthesizing CaO nanoparticles. The antibacterial studies of CaGT and CaP indicated that the synthesized nanoparticles showed sensitivity to both Gram negative and Gram positive bacteria. CaP nanoparticles showed higher photocatalytic activity than CaGT nanoparticles. Hence, calcium oxide nanoparticles synthesized using papaya leaves acts as an excellent photocatalyst in for degradation of dyes from textile industries. REFERENCES [1]. N.Madhusudhana, K.Yogendra and K.Mahadevan, A comparative study on Photocatalytic degradation of Violet GL2B azo dye using CaO and TiO2 nanoparticles. Int J Eng Res Appl, 2(5), 2012, 1300-1307. [2]. A.Roy, S . Samiran, M .Bhattacharya,.; J. Bhattacharya, Antimicrobial Activity of CaO Nanoparticles. J Biomed Nanotechnol. 9(9), 2013,1–8. [3]. X. B Hai, Z. S Xiao, H. L Xiao and Y. L Sheng, Synthesis of porous CaO microsphere and its application in catalyzing transesterification reaction for biodiesel. Trans. Nonferrous Met, 19(3), 2009, 674-77. [4]. N.Madhusudhana.; K.Yogendra and K. M Mahadevan.. Decolorization of Coralene Dark Red 2B azo dye using Calcium Oxide Nanoparticle as an adsorbent. Int. J. Res. Chem. Environ., 2(2), 2012, 21-25. [5]. S. Priscilla Prabhavathi, Ranjith, Shameela Rajam, Maruthamuthu and Kingsley Raja, sol-gel methods of synthesis of MgO and CaO nanoparticles and their characterization. World Journal of Pharmaceutical Research., 3(7), 2014, 362–370. [6]. C. Bhavya and K.Yogendra. Study on The Synthesis,“Characterization and Photocatalytic Activity of CaO Nanoparticle Against Some Selected Azo Dyes, Indian Journal of Applied Research, 5(6) 2015, 361–365.