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N. Gandhi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72

RESEARCH ARTICLE

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OPEN ACCESS

Microwave-Mediated Green Synthesis of Silver Nanoparticles
Using Ficus Elastica Leaf Extract and Application in Air
Pollution Controlling Studies
N. Gandhi, D. Sirisha* and Vikas Chandra Sharma
Center for Environment and Climate Change, Jawaharlal Nehru Institute of Advanced Studies (JNIAS),
Hyderabad, A.P

ABSTRACT
Silver Nanoparticles are applied in various fields due to its anti bacterial properties. A conventional method for
synthesis of AgNP requires dangerous chemical and large amount of energy is released in the process.
Environmental friendly techniques are adopted for the synthesis of nanoparticles of silver. The present research
work summarizes the green synthesis of silver nanoparticles by using leaf extract of Ficus Elastica and
alternative energy sources micro wave irradiation. The synthesized Nanoparticles are characterized by uvvisible spectroscopy and by SEM. The synthesized nanoparticles are applied for controlling SO 2 and NO2 from
aqueous solution of SO2 and NO2. Batch adsorption studies are carried out. The effect of the temperature on
adsorption of aqueous solution is studied at different temperature. A comparison of kinetic models applied to the
adsorption of on silver Nanoparticles was evaluated for the pseudo first order, pseudo second order, Elovich and
intraparticle diffusion models respectively. Results show that pseudo second order model was found to correlate
the experimental data. Data fitted perfectly into and Freundlich adsorption isotherms.
Key words: Batch adsorption, green synthesis, silver Nanoparticles, adsorption kinetics, adsorption isotherms.

I.

Introduction

“Pollution” is the unwanted alteration in
environmental parameters by means of mixing of
certain objects, called as pollutants. Among all the
kinds of pollution, air pollution is one, and has the
deploying impacts over humans and atmosphere.
There are several techniques available to control air
pollution but application of nanotechnology in
environmental pollution control even in initial stage
only. Nanotechnology is one of the modern and
sophisticated technologies which create waves in the
modern times. The opportunities for novel
application continuous to grow as more and more
knowledge are obtained about the Nanoparticles of
Ag. The promise of these developments appears to be
able to enhance the quality of life through novel
applications of nonmaterials. The ability to produce
efficiently and light weight of significant interest of
research. Taking that factor into consideration, the
present study and application of air pollutant
dissolved in aqueous solution.
There are so many ways to synthesize
nanoparticles, but greater emphasis is given on
“Biobased microwave synthesis”. In present study,
the AgNPs were synthesized by using leaf extract of
Ficus elastica with reference of previously done
studies such as by using leaf extract of Acalypha
indica [1], Helianthus annus [2], Pine [3], Moringa
oleifera [4], Camellia sinensis [5], Trianthema
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decandra [6]. The physical characterization of
synthesized AgNPs was done by scanning electron
microscope (SEM) and UV- Vis, Spectrophotometer.
The present study deals with the removal of
NO2 & SO2 from atmosphere. The reason behind
selection of these gases is their carcinogenic trait.
These gases are found to cause cancer especially
breast cancer [7], lungs cancer & cardiac disorders
[8], mainly in the industrial surrounding localities.

II.

Materials and Methods

Preparation of Adsorbent (Ag Nanoparticles)
Source of AgNO3
Chemicals used in the present study all are
including silver nitrate are analytical grade and used
as it is. There is no further purification procedures are
followed.
Preparation of Leaf Extract:
The fresh leaves of Ficus elastica were
collected from vikarabad forest, located 40 km away
from Hyderabad. The leaves were washed with tap
water as well as distilled water to remove dust
particles which present on the surface of leaves. Then
leaves were allowed for dry for 20 minutes then
weighed 25 grams of leaves and grinded it by using
laboratory mortar and pestle. The leaf extract
collected in a 25 ml standard flask and kept in
refrigerator for further use.
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ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72
Preparation of Silver Nanoparticles:
Many techniques, including chemical and
physical means, have been to prepare metal
nanoparticles, such as chemical reduction using a
reducing agent, electrochemical reduction, photo
chemical reduction and heat evaporation method. Not
only physicists and chemists, but also the biologists
are highly interested in synthesizing nanoparticles of
different shapes and sized by employing bio-based
synthesis of nanometals using plant leaf extracts. In
the present study to the 25 ml leaf extract 100 ml of
0.1 M AgNO3 solution was added and kept it in
microwave oven at 180 watts for 30 minutes.
Formations of silver nanoparticles were checked by
using UV-vis spectrophotometer (Lambda Scientific
Spectrophotometer) at regular intervals. This
naturally occurring nanoparticles are generated by the
erosion and chemical degradation of plants [9].
Characterization of Silver Nanoparticles:
The characterization technique involves UVvis absorption spectra, Scanning Electron Microscope
(SEM), Fourier transform infrared spectroscopy (FTIR).
Preparation of Standard Samples:
A 100 ppm stock solution of Sulphite
prepared by dissolving 0.1575 gm of Analytical
grade Sodium sulphite in double distilled water and
made up to 1000 ml with double distilled water. A
100 ppm stock solution of nitrite prepared by
dissolving 177 mg of Analytical grade sodium nitrite
in 1000 ml standard flask and made up to the mark
with double distilled water. From the stock solution
of Sulphite and Nitrite the working standards are
prepared by taking appropriate quantities to get the
desire concentration of SO2 and NO2. The working
standards are treated with silver nanoparticles and
checked for percentage removal by using Uv-Vis
Spectrophotometer. Batch Adsorption Studies are
carried out for the removal of SO2 and NO2. The
percentage removal of SO2 and NO2 is calculated by
using the following formula.
% Removal = Initial Concentration – Final
Concentration X 100
Initial Concentration
Experimental Procedure:
In the present study an attempt has been
made to suggest a new method application on green
synthesized silver nanoparticles in air pollution
controlling
technologies.
Batch
adsorption
experiments were adopted for the removal studies.
The estimation of SO2 is done by west geak method
and NO2 estimation by NEDA method. The
experiments are conducted with respect to contact

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time, effect of SO2 concentrations,
nanoparticles dosage and temperature effect.

silver

Effect of Contact time and Kinetic models:
Contact time plays an important role in
designing the system [10]. The initial (before batch
adsorption) and final (after batch adsorption)
concentrations of SO2 and NO2 are determined at
regular time intervals i.e. 5, 10, 15, 20, 30, 40, 45, 50
and 60 minutes. In order to investigate the
mechanism of adsorption several kinetic models were
tested including pseudo first order kinetic model, the
Elovich model and pseudo second order kinetic
model for batch adsorption studies [11].
Effect of Initial concentrations of SO2 on Silver
nanoparticles:
Different concentrations of aqueous
solutions of SO2 were studied with a constant amount
of adsorbent (silver nanoparticles) and constant
contact time. The initial and final concentrations of
SO2 were determined by spectrophotometer. The
results are given in figure-12.
Effect of Adsorbent Dosage:
To a series of constant concentrations of
SO2 solutions, different amount of adsorbent were
added and allowed it for batch adsorption for 60
minutes to get equilibrium. After batch adsorption
samples were tested for percentage removal by using
spectrophotometer.
Effect of Temperature
To study the effect of temperature, the
experiments are conducted at following temperature
0, 20, 40, 60, 80 and 100 O C.
Initial screenings have been done by taking both SO2
and NO2 separately. Finally it was observed that
decrease in SO2 concentration but there is no change
in NO2 concentration. It means silver nanoparticles
do not have the capacity to remove aqueous NO2
solution. So effects of contact time, concentration and
adsorbent dosage have done by taking only with SO2
solution.

III.

Results and Discussion

UV- Visible Analysis of Silver Nanoparticles
The distinctive colors of colloidal silver are
due to a phenomenon known as Plasmon absorbance.
Incident light creates oscillation in conduction
electrons on the surface of the nanoparticles and
electromagnetic radiation is absorbed. The spectrum
of clear brownish green colloidal silver from the
synthesis. The Plasmon resonance produces a peak
near 400 nm. It is already been reported that the
absorption spectrum of aqueous AgNO3 only solution
exhibited λ max at about 220 nm where as silver
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N. Gandhi et al Int. Journal of Engineering Research and Applications
ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72
nanoparticles λ max at about 430 nm [2]. The
wavelength of the Plasmon absorption maximum in a
given solvent can be used to indicate particle size. If
the λ max in between 395 nm- 405 nm then the size
of the particle is in between 10-14 nm, if the λ max
420 nm then the particle size is in between 35-50 nm
and the λ max 438-440 indicates that the formed
nanoparticles are around 60-80 nm in size.
Thus, color change of the solution clearly
indicated the formation of AgNPs. The color
intensity of the cell filtrate with AgNO 3 was
sustained even after 24 h incubation, which indicated

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that the particles were well dispersed in the solution,
and there was no obvious aggregation .All these
reactions were monitored by ultraviolet-visible
spectroscopy of the colloidal AgNPs solutions. The
ultraviolet-visible spectra of the cell filtrate with
AgNO3 showed a strong broad peak at 430 nm which
is surface Plasmon resonances (SPR band), which
indicated the presence of AgNPs (Figure). These
results were consistent with the reports of Verma et al
2010 [12]. The intensity of the SPR band steadily
increased from 15 min to 25 min as a function of time
of reaction.

O.D

Figure-1: Graphical form of absorbances for synthesis of AgNPs by using Ficus elastica leaf extract

500
450
400
350
300
250
200
150
100
50
0
0

15
20
25
time in minute
Figure-2: Graphical form of Relationship between λ and time of introduction
max

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5

10

30

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ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72

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Figure-3: Change in colour of Ficus elastica leaf extract during nanoparticle synthesis
From the figure-3 and graph it was
concluded that the formed particles are silver
nanoparticles with the size around 50-60 nm. The
application of AgNPs was highly dependent on the
chemical
composition,
shape,
size,
and
monodispersity of particles [13] to broaden the
application scope; the AgNPs obtained were
systematically characterized using SEM and FT-IR
analysis. Through the SEM analysis, the particles
were spherical and polydisperse with an average size
of 50 nm, and the majority of the particles were less
than 50 nm.

Particle Size Measurement using SEM
Silver nanoparticles that produced the
spectrum were examined using Scanning Electron
Microscopy. A sample of silver nanoparticles from
freshly prepared clear brownish green solution was
centrifuged at 8000 rpm for 5 minutes and
redispersed in distilled water. This procedure was
repeated three times and the remnant pellets were
dried and powdered for SEM analysis. A thin film of
the sample was prepared by dissolving a portion of
the powdered particle in sterile distilled water on
small glass cover slip and set on a copper stab for
electron microscopy. The results are given in figure4.

Figure-4: SEM image of synthesized silver nanoparticles. Fourier transforms infrared
spectroscopy (FTIR) Analysis

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Figure-5: FT-IR analysis plot of Synthesized Silver Nanoparticles:
are responsible for the reduction of metal ions when
FTIR studies are carried for identifying the
using leaf extract. The peaks arise due to carbonyl
bio molecules responsible for capping and reducing
stretch and N-H stretch in vibrations in the amide
AgNPs from the extract. The peaks at 3436.9 and
linkage of the proteins. The study confirms amino
2917.1 were due to the stretching of primary and
groups and peptide bonds of proteins form a capping
secondary amides respectively [14]. The peaks at
agent and maintaining the stability [15-17].
these two regions are characteristic of proteins that
3.1 Effect of Contact time and Kinetic studies
105

% R em oval

100

5 p p m c o n c e n t r a t io n s o lu t io n
1 0 p p m c o n c e n tr a tio n s o lu t io n
1 5 p p m c o n c e n tr a tio n s o lu t io n

95

90

85
0

5

10

15

20

25

30

35

40

45

50

55

60

C o n t a n c t t im e ( in m in )

Fig- 6: Variation of contact time on SO2 removal
From the figure-6, it was observed that the
percentage removal of aqueous SO2 is increasing
with increase in contact time and it became constant
at optimum contact time [18]. The experiment was
performed taking three different concentration of SO 2
solution and checked for contact time effect and it is
showing same results for all three different
concentrations. The initial rapid adsorption showed a
very slow approach to equilibrium. The nature of
adsorbent and its available sorption sites affected the

Kinetic Studies
In order to check the kinetic parameters of
removal of SO2 using silver nanoparticles, the
experimental data were tested with pseudo first order
kinetic model, pseudo second order kinetic model
and Elovich kinetic model. This adsorption kinetics is
used to investigate the mechanism and the rate
controlling steps of adsorption. The mechanism of
adsorption involves the chemical reaction of
functional groups present on the surface of the
adsorbent and the adsorbate, temperature [20].

time needed to reach equilibrium [19], for silver
nanoparticles this time was 5 minutes.

Pseudo first order kinetic model
This model explains that the rate of change
of solute uptake with time is directly proportional to

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difference in saturation concentration and the amount
of solid uptake with time [21]. The plot of log (qe –
qt) versus t should give a straight line with slope of –
k/2.303 and intercept log qe. Where qe and qt are the
amount of SO2 adsorbed at equilibrium and at contact
time t. From the slope and intercept of the plot the

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adsorption rate constant and equilibrium adsorption
capacity were calculated [20]. From the graph
(Figure- 7) and statistical report (Table-1) it was
observed the present study removal of SO2 by silver
nanoparticles is following pseudo first order kinetic
model.

0 .5

5ppm

C o n ta c t tim e (in m in )

10ppm

lo g ( q e - q t )

0 .0
5

10

15

20

25

30

35

40

45

15ppm

50

- 0 .5

- 1 .0

- 1 .5

Figure- 7: Graphical representation of Pseudo first order kinetic model
Pseudo Second order kinetic model
The pseudo second order kinetic order
equation expressed as
t/qt = 1 + t/qe
k2qe2
Where k2 is the rate constant of pseudo second order
adsorption (g/mg min) and qe is the equilibrium
adsorption capacity (mg/gm) [22]. Figure-8 shows
the pseudo second order plot for the adsorption of
SO2 using silver nanoparticles at different initial
concentration at room temperature.

When the pseudo second order kinetic is applicable,
the plot of t/qt against t should give a linear
relationship from which k2 and qe determined
respectively from the intercept and slope of the plot.
The figure showing the plot of pseudo second order
kinetic model with linear relation. The r2 values are
higher than the values of pseudo first order kinetic
model. It is observed form the figure that the
adsorption of SO2 by silver nanoparticles perfectly
fits to the pseudo second order kinetic model.

15

5ppm

10

t/q t

10ppm
15ppm

5

0
10

20

30

40

50

60

C o n t a c t t im e ( in m in )

Figure- 8: Graphical representation of Pseudo second order kinetic model
Elovich Model
The Elovich model equation is generally
expressed as [23-24]
dqt/dt = α exp (-β qt)
Where:
α is the initial adsorption rate (mg·g-1·min-1)
β is the desorption constant (g·mg-1) during any one
experiment.
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If the adsorption of aqueous SO2 solution by
silver nanoparticles fits to the Elovich model, a plot
of qt versus In(t) should give a linear relationship
with a slope of (1/β) and an intercept of 1/β In (αβ).
The results of Elovich plot for the adsorption of SO 2
by silver nanoparticles at various initial
concentrations are given in figure-9. Form the table-1
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and figure-9 it was observed that the Elovich model
does not fit for the adsorption of SO2 by silver

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nanoparticles. The Elovich model mainly applicable
for chemical adsorption kinetics [25].

20

5ppm
10ppm

15

qt

15ppm
10

5

0
0

1

2

3

4

5

ln t

Figure- 9: Graphical representation of Elovich kinetic model
Intra particle diffusion model analysis
The adsorption of aqueous SO2 solution by
silver nanoparticles fits into pseudo second order
kinetic model. To find out the adsorption mechanism
the data is tested with intra particle diffusion model.
Adsorption is a multi step process involving transport
of the solute molecules from the aqueous phase to the
surface of the solid particulates followed by diffusion
into the interior of the pores [20]. Assuming that the
rate is controlled by pore and intra particle diffusion,
the amount adsorbed (qt) is proportional to the t1/2, as
shown below

qt = kidt1/2 + I
where qt is the amount of SO2 adsorbed (mg/g) at
time t (min), and I is the intercept (mg/g). kid and I
values are obtained from the slopes and intercept of
the linear plot. Figure-10 represents the plots of qt
versus t1/2 for adsorption of SO2 by silver
nanoparticles at various initial SO2 concentrations.
From the figure and table it was observed that the
adsorption mechanism is not fits to intra particle
diffusion model.

20

5ppm
10ppm

qt

15

15ppm

10

5

0
0

2

4

6

(t)

8

10

1 /2

Figure-10: Intraparticle diffusion plots for the removal SO 2 by silver nanoparticles.
increase or decrease. In present study (Figure-11) the
3.2 Effect of Initial Concentration of SO2 on
percentage removal of aqueous SO2 solution is
AgNps
The Adsorptive removal of SO2 from
decreases with increase in initial concentration of
aqueous solution is purely depends on the
SO2 solution [26]. However at higher concentration
concentration SO2 and available binding sites of
the available sites of adsorption becomes fewer and
adsorbent and its nature. If the concentration of SO 2
the
percentage
of
removal
is
decrease.
is increased the percentage of removal might be

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120

% r e m o v a l w ith 0 .1 g m A g N P s
% r e m o v a l w ith 0 .2 g m A g N P s

% re m o v a l

100

80

60

40
0

20

40

60

C o n c e n tr a t io n in p p m

Figure-11: Effect of initial SO2 concentration on adsorption process
3.3 Effect of Adsorbent Dosage
Figure- shows the effect of adsorbent dosage
on the percentage adsorption. From the figure it was
observed that the percentage removal of aqueous SO2
is increasing with increase adsorbent dosage and it
became constant at optimum adsorbent dosage of 0.3

gm/ 100 ml of 10 ppm concentrated solution. The
reason behind this study the initial concentration of
SO2 is constant and the amount of silver
nanoparticles are varies so the availability of binding
sites are more.

% Rem oval

100

90

80

70
0 .0

0 .2

0 .4

C o n c e n tr a tio n

in

0 .6

p p m

Figure-12: Effect of adsorbent dosage on SO2 removal
3.4 Effect of Temperature
Temperature has an important effect on the
process of adsorption. The percentage of SO2
adsorption is studied as a function of temperature.
The results obtained are presented in figure-13 at
temperatures of 0oC, 40oC, 60oC, 80oC and 100oC.

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The decrease in percentage of adsorption with rise in
temperature may be due to desorption caused by an
increase in the available thermal energy. Higher
temperature induces higher mobility of the adsorbate
causing desorption [27].

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105

1ppm

% Rem oval

2ppm
3ppm

100

4ppm
5ppm
95

90
0

20

40

60

80

100

T e m p e r a t u r e ( C )

Figure- 13: Effect of Temperature on Adsorption of SO 2
3.5 Adsorption isotherms
3.5.1
Langmuir adsorption isotherm
The Langmuir adsorption isotherm is the
best known linear model to determine the adsorption
parameters. Langmuir model represented by
following equation
qe = KL Ce = Q0bCe
1+ bLCe 1+ bLCe
The linearized form of Langmuir adsorption
isotherm is as follows

Ce =

1
+ (1/Q0) Ce
Q0bL
Where qe is the amount adsorbed at equilibrium
(mg/g), Q0 is the monolayer adsorption capacity
(9mg/g), Ce the equilibrium concentration of
adsorbate (mg/L) and bL is the Langmuir constant
related to energy adsorption. The figure-14 shows the
plot of Ce/qe against Ce. Values of Q0 and bL are in
table-2. From the figure-14 and table-2 it was
observed that the adsorption isotherm studies of
removal of SO2 by silver nanoparticles does not fit
for the Langmuir isotherm.

1 .1 0

0 C
40 C

1 .0 5

C e /q e

60 C
80 C

1 .0 0

0 .9 5

0 .9 0
0

2

4

6

Ce

Figure-14: Langmuir adsorption plot for SO2 removal at different temperature
3.5.2
Freundlich adsorption isotherm
The Freundlich equation is an empirical
relationship describing the adsorption of solute from
liquid to a solid surface. The Freundlich equation is
expressed as
qe = kf Ce1/n
The linear form of Freundlich equation is as follows
Log qe = log kf + 1/n (log Ce)

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Where kf is the Freundlich adsorption capacity and n
is the adsorption intensity. A plot of log q e versus log
Ce gives a linear line with slope of 1/n and intercept
of log kf given in table-2. From the figure-15 and
table-2 it was observed that the adsorption of aqueous
SO2 at different temperature perfectly fits in to
Freundlich isotherm. The r2 value and ASS, values
are more comparing to Langmuir isotherms.

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0 .8

0 C
40 C

0 .6

lo g q e

60 C
80 C

0 .4

0 .2

0 .0
0 .0

0 .2

0 .4

0 .6

0 .8

lo g C e

Figure-15: Freundlich adsorption isotherm plots of SO2 removal at different temperature
3.5.3

Temkin adsorption isotherm
6

0 C
40 C
60 C

4

Ce

80 C
2

0
0

2

4

6

x /m

Figure-16: Temkin adsorption isotherm plots of SO2 removal at different temperature.
Temkin adsorption isotherm is studied by
takes into account he interactions between adsorbents
and metal ions to be adsorbed and is based on the
assumption that the free energy of sorption is a
function of the surface coverage [28]. The linear form
of the Temkin isotherm is represented as:
qe = B ln A + B ln Ce

Where Ce is the equilibrium concentration of the
adsorbate in mg/L, qe is the amount of adsorbate
adsorbed at equilibrium (mg/g), RT/bT= B where T is
the temperature (K) and R is the ideal gas constant
(8.314 J mol-1K-1) and A and bT are constants. Figure16 showing relation between Ce and qe, from the
figure-16 and table-2 it was observed that the
adsorption of SO2 by silver nanoparticles is following
Temkin adsorption isotherms.

Table-1: Kinetic parameters for adsorption of Aqueous SO2 by Silver Nanoparticles
S.No

Parameters

01

R2
ASS
K1

02

R2
ASS
K2

03

R2
ASS
α
β

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SO2concentration
SO2 concentration
(5 ppm/L)
(10 ppm/L)
Pseudo first order kinetic model
0.999
0.999
0.0
0.0
0.0625
0.0835
Pseudo Second order kinetic model
0.999
0.999
0.0505
0.0389
3.8196 X 10-3
10.2208 X 10-3
Elovich model
0.6788
0.6921
0.01285
0.1484
3.067 X 10-6
4.2026 X 10-6
92.2509
27.173

SO2 concentration
(15 ppm/L)
0.8751
0.1062
0.1054
0.999
0.0167
5.4111 X 10-3
0.7867
0.3015
2.3743 X 10-6
19.033

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04

Intraparticle diffusion model
0.4286
0.02285
0.03969
0.008685

R2
ASS
kid
I

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0.4409
0.2695
0.1363
0.02982

0.5370
0.6546
0.2124
0.04648

Table-2: Isotherm kinetics for adsorption of Aqueous SO 2 by Silver Nanoparticles
S.No

Parameters
0

01

R2
ASS
aT
bT

0.999
0.0240
0.003618
0.001093

02

R2
ASS
Q0
bL

0.05357
0.01071
0.002415
0.0007280

03

R2
ASS
kf
n

0.999
0.0147
0.001236
0.002558

IV.

Temperature oC
40
60
Temkin Adsorption Isotherm
0.999
0.999
0.0240
0.0240
0.003618
0.003618
0.001093
0.001093
Langmuir Adsorption Isotherm
0.05357
0.05357
0.01071
0.01071
0.002415
0.002415
0.0007280
0.0007280
Freundlich Adsorption Isotherm
0.999
0.999
0.0147
0.0147
0.001236
0.001236
0.002558
0.002558

Conclusion

In this study, silver nanoparticles are
synthesized by Ficus Elastica using the alternative
energy source of microwave irradiation. The AgNPs
are highly stable AgNPs synthesized in the present
study are capable of adsorbing SO2 molecules from
aqueous solution and these AgNPs are inefficient in
adsorbing NO2. The formation of silver nanoparticles
is confirmed by SEM and spectrophotometrically.
Investigation carried out on adsorption studies
revealed that it is following Pseudo second order
kinetics. Optimum dosage for 98% removal of SO2 is
equal to ecofriendly nontoxic energy saving method
is employed in the synthesis of nanoparticles. The
present study gives a new direction for developing a
catalytic tube for controlling air pollutant SO 2 caused
by petrol-drove vehicles.

V.

Acknowledgement

[2]

[3]

[4]

[5]

The authors are sincerely thankful to Mrs.
Sujatha Gangadhar, registrar JNIAS for her constant
encouragement and for financial support for
completing this project.

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  • 1. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 RESEARCH ARTICLE www.ijera.com OPEN ACCESS Microwave-Mediated Green Synthesis of Silver Nanoparticles Using Ficus Elastica Leaf Extract and Application in Air Pollution Controlling Studies N. Gandhi, D. Sirisha* and Vikas Chandra Sharma Center for Environment and Climate Change, Jawaharlal Nehru Institute of Advanced Studies (JNIAS), Hyderabad, A.P ABSTRACT Silver Nanoparticles are applied in various fields due to its anti bacterial properties. A conventional method for synthesis of AgNP requires dangerous chemical and large amount of energy is released in the process. Environmental friendly techniques are adopted for the synthesis of nanoparticles of silver. The present research work summarizes the green synthesis of silver nanoparticles by using leaf extract of Ficus Elastica and alternative energy sources micro wave irradiation. The synthesized Nanoparticles are characterized by uvvisible spectroscopy and by SEM. The synthesized nanoparticles are applied for controlling SO 2 and NO2 from aqueous solution of SO2 and NO2. Batch adsorption studies are carried out. The effect of the temperature on adsorption of aqueous solution is studied at different temperature. A comparison of kinetic models applied to the adsorption of on silver Nanoparticles was evaluated for the pseudo first order, pseudo second order, Elovich and intraparticle diffusion models respectively. Results show that pseudo second order model was found to correlate the experimental data. Data fitted perfectly into and Freundlich adsorption isotherms. Key words: Batch adsorption, green synthesis, silver Nanoparticles, adsorption kinetics, adsorption isotherms. I. Introduction “Pollution” is the unwanted alteration in environmental parameters by means of mixing of certain objects, called as pollutants. Among all the kinds of pollution, air pollution is one, and has the deploying impacts over humans and atmosphere. There are several techniques available to control air pollution but application of nanotechnology in environmental pollution control even in initial stage only. Nanotechnology is one of the modern and sophisticated technologies which create waves in the modern times. The opportunities for novel application continuous to grow as more and more knowledge are obtained about the Nanoparticles of Ag. The promise of these developments appears to be able to enhance the quality of life through novel applications of nonmaterials. The ability to produce efficiently and light weight of significant interest of research. Taking that factor into consideration, the present study and application of air pollutant dissolved in aqueous solution. There are so many ways to synthesize nanoparticles, but greater emphasis is given on “Biobased microwave synthesis”. In present study, the AgNPs were synthesized by using leaf extract of Ficus elastica with reference of previously done studies such as by using leaf extract of Acalypha indica [1], Helianthus annus [2], Pine [3], Moringa oleifera [4], Camellia sinensis [5], Trianthema www.ijera.com decandra [6]. The physical characterization of synthesized AgNPs was done by scanning electron microscope (SEM) and UV- Vis, Spectrophotometer. The present study deals with the removal of NO2 & SO2 from atmosphere. The reason behind selection of these gases is their carcinogenic trait. These gases are found to cause cancer especially breast cancer [7], lungs cancer & cardiac disorders [8], mainly in the industrial surrounding localities. II. Materials and Methods Preparation of Adsorbent (Ag Nanoparticles) Source of AgNO3 Chemicals used in the present study all are including silver nitrate are analytical grade and used as it is. There is no further purification procedures are followed. Preparation of Leaf Extract: The fresh leaves of Ficus elastica were collected from vikarabad forest, located 40 km away from Hyderabad. The leaves were washed with tap water as well as distilled water to remove dust particles which present on the surface of leaves. Then leaves were allowed for dry for 20 minutes then weighed 25 grams of leaves and grinded it by using laboratory mortar and pestle. The leaf extract collected in a 25 ml standard flask and kept in refrigerator for further use. 61 | P a g e
  • 2. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 Preparation of Silver Nanoparticles: Many techniques, including chemical and physical means, have been to prepare metal nanoparticles, such as chemical reduction using a reducing agent, electrochemical reduction, photo chemical reduction and heat evaporation method. Not only physicists and chemists, but also the biologists are highly interested in synthesizing nanoparticles of different shapes and sized by employing bio-based synthesis of nanometals using plant leaf extracts. In the present study to the 25 ml leaf extract 100 ml of 0.1 M AgNO3 solution was added and kept it in microwave oven at 180 watts for 30 minutes. Formations of silver nanoparticles were checked by using UV-vis spectrophotometer (Lambda Scientific Spectrophotometer) at regular intervals. This naturally occurring nanoparticles are generated by the erosion and chemical degradation of plants [9]. Characterization of Silver Nanoparticles: The characterization technique involves UVvis absorption spectra, Scanning Electron Microscope (SEM), Fourier transform infrared spectroscopy (FTIR). Preparation of Standard Samples: A 100 ppm stock solution of Sulphite prepared by dissolving 0.1575 gm of Analytical grade Sodium sulphite in double distilled water and made up to 1000 ml with double distilled water. A 100 ppm stock solution of nitrite prepared by dissolving 177 mg of Analytical grade sodium nitrite in 1000 ml standard flask and made up to the mark with double distilled water. From the stock solution of Sulphite and Nitrite the working standards are prepared by taking appropriate quantities to get the desire concentration of SO2 and NO2. The working standards are treated with silver nanoparticles and checked for percentage removal by using Uv-Vis Spectrophotometer. Batch Adsorption Studies are carried out for the removal of SO2 and NO2. The percentage removal of SO2 and NO2 is calculated by using the following formula. % Removal = Initial Concentration – Final Concentration X 100 Initial Concentration Experimental Procedure: In the present study an attempt has been made to suggest a new method application on green synthesized silver nanoparticles in air pollution controlling technologies. Batch adsorption experiments were adopted for the removal studies. The estimation of SO2 is done by west geak method and NO2 estimation by NEDA method. The experiments are conducted with respect to contact www.ijera.com www.ijera.com time, effect of SO2 concentrations, nanoparticles dosage and temperature effect. silver Effect of Contact time and Kinetic models: Contact time plays an important role in designing the system [10]. The initial (before batch adsorption) and final (after batch adsorption) concentrations of SO2 and NO2 are determined at regular time intervals i.e. 5, 10, 15, 20, 30, 40, 45, 50 and 60 minutes. In order to investigate the mechanism of adsorption several kinetic models were tested including pseudo first order kinetic model, the Elovich model and pseudo second order kinetic model for batch adsorption studies [11]. Effect of Initial concentrations of SO2 on Silver nanoparticles: Different concentrations of aqueous solutions of SO2 were studied with a constant amount of adsorbent (silver nanoparticles) and constant contact time. The initial and final concentrations of SO2 were determined by spectrophotometer. The results are given in figure-12. Effect of Adsorbent Dosage: To a series of constant concentrations of SO2 solutions, different amount of adsorbent were added and allowed it for batch adsorption for 60 minutes to get equilibrium. After batch adsorption samples were tested for percentage removal by using spectrophotometer. Effect of Temperature To study the effect of temperature, the experiments are conducted at following temperature 0, 20, 40, 60, 80 and 100 O C. Initial screenings have been done by taking both SO2 and NO2 separately. Finally it was observed that decrease in SO2 concentration but there is no change in NO2 concentration. It means silver nanoparticles do not have the capacity to remove aqueous NO2 solution. So effects of contact time, concentration and adsorbent dosage have done by taking only with SO2 solution. III. Results and Discussion UV- Visible Analysis of Silver Nanoparticles The distinctive colors of colloidal silver are due to a phenomenon known as Plasmon absorbance. Incident light creates oscillation in conduction electrons on the surface of the nanoparticles and electromagnetic radiation is absorbed. The spectrum of clear brownish green colloidal silver from the synthesis. The Plasmon resonance produces a peak near 400 nm. It is already been reported that the absorption spectrum of aqueous AgNO3 only solution exhibited λ max at about 220 nm where as silver 62 | P a g e
  • 3. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 nanoparticles λ max at about 430 nm [2]. The wavelength of the Plasmon absorption maximum in a given solvent can be used to indicate particle size. If the λ max in between 395 nm- 405 nm then the size of the particle is in between 10-14 nm, if the λ max 420 nm then the particle size is in between 35-50 nm and the λ max 438-440 indicates that the formed nanoparticles are around 60-80 nm in size. Thus, color change of the solution clearly indicated the formation of AgNPs. The color intensity of the cell filtrate with AgNO 3 was sustained even after 24 h incubation, which indicated www.ijera.com that the particles were well dispersed in the solution, and there was no obvious aggregation .All these reactions were monitored by ultraviolet-visible spectroscopy of the colloidal AgNPs solutions. The ultraviolet-visible spectra of the cell filtrate with AgNO3 showed a strong broad peak at 430 nm which is surface Plasmon resonances (SPR band), which indicated the presence of AgNPs (Figure). These results were consistent with the reports of Verma et al 2010 [12]. The intensity of the SPR band steadily increased from 15 min to 25 min as a function of time of reaction. O.D Figure-1: Graphical form of absorbances for synthesis of AgNPs by using Ficus elastica leaf extract 500 450 400 350 300 250 200 150 100 50 0 0 15 20 25 time in minute Figure-2: Graphical form of Relationship between λ and time of introduction max www.ijera.com 5 10 30 63 | P a g e
  • 4. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 www.ijera.com Figure-3: Change in colour of Ficus elastica leaf extract during nanoparticle synthesis From the figure-3 and graph it was concluded that the formed particles are silver nanoparticles with the size around 50-60 nm. The application of AgNPs was highly dependent on the chemical composition, shape, size, and monodispersity of particles [13] to broaden the application scope; the AgNPs obtained were systematically characterized using SEM and FT-IR analysis. Through the SEM analysis, the particles were spherical and polydisperse with an average size of 50 nm, and the majority of the particles were less than 50 nm. Particle Size Measurement using SEM Silver nanoparticles that produced the spectrum were examined using Scanning Electron Microscopy. A sample of silver nanoparticles from freshly prepared clear brownish green solution was centrifuged at 8000 rpm for 5 minutes and redispersed in distilled water. This procedure was repeated three times and the remnant pellets were dried and powdered for SEM analysis. A thin film of the sample was prepared by dissolving a portion of the powdered particle in sterile distilled water on small glass cover slip and set on a copper stab for electron microscopy. The results are given in figure4. Figure-4: SEM image of synthesized silver nanoparticles. Fourier transforms infrared spectroscopy (FTIR) Analysis www.ijera.com 64 | P a g e
  • 5. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 www.ijera.com Figure-5: FT-IR analysis plot of Synthesized Silver Nanoparticles: are responsible for the reduction of metal ions when FTIR studies are carried for identifying the using leaf extract. The peaks arise due to carbonyl bio molecules responsible for capping and reducing stretch and N-H stretch in vibrations in the amide AgNPs from the extract. The peaks at 3436.9 and linkage of the proteins. The study confirms amino 2917.1 were due to the stretching of primary and groups and peptide bonds of proteins form a capping secondary amides respectively [14]. The peaks at agent and maintaining the stability [15-17]. these two regions are characteristic of proteins that 3.1 Effect of Contact time and Kinetic studies 105 % R em oval 100 5 p p m c o n c e n t r a t io n s o lu t io n 1 0 p p m c o n c e n tr a tio n s o lu t io n 1 5 p p m c o n c e n tr a tio n s o lu t io n 95 90 85 0 5 10 15 20 25 30 35 40 45 50 55 60 C o n t a n c t t im e ( in m in ) Fig- 6: Variation of contact time on SO2 removal From the figure-6, it was observed that the percentage removal of aqueous SO2 is increasing with increase in contact time and it became constant at optimum contact time [18]. The experiment was performed taking three different concentration of SO 2 solution and checked for contact time effect and it is showing same results for all three different concentrations. The initial rapid adsorption showed a very slow approach to equilibrium. The nature of adsorbent and its available sorption sites affected the Kinetic Studies In order to check the kinetic parameters of removal of SO2 using silver nanoparticles, the experimental data were tested with pseudo first order kinetic model, pseudo second order kinetic model and Elovich kinetic model. This adsorption kinetics is used to investigate the mechanism and the rate controlling steps of adsorption. The mechanism of adsorption involves the chemical reaction of functional groups present on the surface of the adsorbent and the adsorbate, temperature [20]. time needed to reach equilibrium [19], for silver nanoparticles this time was 5 minutes. Pseudo first order kinetic model This model explains that the rate of change of solute uptake with time is directly proportional to www.ijera.com 65 | P a g e
  • 6. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 difference in saturation concentration and the amount of solid uptake with time [21]. The plot of log (qe – qt) versus t should give a straight line with slope of – k/2.303 and intercept log qe. Where qe and qt are the amount of SO2 adsorbed at equilibrium and at contact time t. From the slope and intercept of the plot the www.ijera.com adsorption rate constant and equilibrium adsorption capacity were calculated [20]. From the graph (Figure- 7) and statistical report (Table-1) it was observed the present study removal of SO2 by silver nanoparticles is following pseudo first order kinetic model. 0 .5 5ppm C o n ta c t tim e (in m in ) 10ppm lo g ( q e - q t ) 0 .0 5 10 15 20 25 30 35 40 45 15ppm 50 - 0 .5 - 1 .0 - 1 .5 Figure- 7: Graphical representation of Pseudo first order kinetic model Pseudo Second order kinetic model The pseudo second order kinetic order equation expressed as t/qt = 1 + t/qe k2qe2 Where k2 is the rate constant of pseudo second order adsorption (g/mg min) and qe is the equilibrium adsorption capacity (mg/gm) [22]. Figure-8 shows the pseudo second order plot for the adsorption of SO2 using silver nanoparticles at different initial concentration at room temperature. When the pseudo second order kinetic is applicable, the plot of t/qt against t should give a linear relationship from which k2 and qe determined respectively from the intercept and slope of the plot. The figure showing the plot of pseudo second order kinetic model with linear relation. The r2 values are higher than the values of pseudo first order kinetic model. It is observed form the figure that the adsorption of SO2 by silver nanoparticles perfectly fits to the pseudo second order kinetic model. 15 5ppm 10 t/q t 10ppm 15ppm 5 0 10 20 30 40 50 60 C o n t a c t t im e ( in m in ) Figure- 8: Graphical representation of Pseudo second order kinetic model Elovich Model The Elovich model equation is generally expressed as [23-24] dqt/dt = α exp (-β qt) Where: α is the initial adsorption rate (mg·g-1·min-1) β is the desorption constant (g·mg-1) during any one experiment. www.ijera.com If the adsorption of aqueous SO2 solution by silver nanoparticles fits to the Elovich model, a plot of qt versus In(t) should give a linear relationship with a slope of (1/β) and an intercept of 1/β In (αβ). The results of Elovich plot for the adsorption of SO 2 by silver nanoparticles at various initial concentrations are given in figure-9. Form the table-1 66 | P a g e
  • 7. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 and figure-9 it was observed that the Elovich model does not fit for the adsorption of SO2 by silver www.ijera.com nanoparticles. The Elovich model mainly applicable for chemical adsorption kinetics [25]. 20 5ppm 10ppm 15 qt 15ppm 10 5 0 0 1 2 3 4 5 ln t Figure- 9: Graphical representation of Elovich kinetic model Intra particle diffusion model analysis The adsorption of aqueous SO2 solution by silver nanoparticles fits into pseudo second order kinetic model. To find out the adsorption mechanism the data is tested with intra particle diffusion model. Adsorption is a multi step process involving transport of the solute molecules from the aqueous phase to the surface of the solid particulates followed by diffusion into the interior of the pores [20]. Assuming that the rate is controlled by pore and intra particle diffusion, the amount adsorbed (qt) is proportional to the t1/2, as shown below qt = kidt1/2 + I where qt is the amount of SO2 adsorbed (mg/g) at time t (min), and I is the intercept (mg/g). kid and I values are obtained from the slopes and intercept of the linear plot. Figure-10 represents the plots of qt versus t1/2 for adsorption of SO2 by silver nanoparticles at various initial SO2 concentrations. From the figure and table it was observed that the adsorption mechanism is not fits to intra particle diffusion model. 20 5ppm 10ppm qt 15 15ppm 10 5 0 0 2 4 6 (t) 8 10 1 /2 Figure-10: Intraparticle diffusion plots for the removal SO 2 by silver nanoparticles. increase or decrease. In present study (Figure-11) the 3.2 Effect of Initial Concentration of SO2 on percentage removal of aqueous SO2 solution is AgNps The Adsorptive removal of SO2 from decreases with increase in initial concentration of aqueous solution is purely depends on the SO2 solution [26]. However at higher concentration concentration SO2 and available binding sites of the available sites of adsorption becomes fewer and adsorbent and its nature. If the concentration of SO 2 the percentage of removal is decrease. is increased the percentage of removal might be www.ijera.com 67 | P a g e
  • 8. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 www.ijera.com 120 % r e m o v a l w ith 0 .1 g m A g N P s % r e m o v a l w ith 0 .2 g m A g N P s % re m o v a l 100 80 60 40 0 20 40 60 C o n c e n tr a t io n in p p m Figure-11: Effect of initial SO2 concentration on adsorption process 3.3 Effect of Adsorbent Dosage Figure- shows the effect of adsorbent dosage on the percentage adsorption. From the figure it was observed that the percentage removal of aqueous SO2 is increasing with increase adsorbent dosage and it became constant at optimum adsorbent dosage of 0.3 gm/ 100 ml of 10 ppm concentrated solution. The reason behind this study the initial concentration of SO2 is constant and the amount of silver nanoparticles are varies so the availability of binding sites are more. % Rem oval 100 90 80 70 0 .0 0 .2 0 .4 C o n c e n tr a tio n in 0 .6 p p m Figure-12: Effect of adsorbent dosage on SO2 removal 3.4 Effect of Temperature Temperature has an important effect on the process of adsorption. The percentage of SO2 adsorption is studied as a function of temperature. The results obtained are presented in figure-13 at temperatures of 0oC, 40oC, 60oC, 80oC and 100oC. www.ijera.com The decrease in percentage of adsorption with rise in temperature may be due to desorption caused by an increase in the available thermal energy. Higher temperature induces higher mobility of the adsorbate causing desorption [27]. 68 | P a g e
  • 9. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 www.ijera.com 105 1ppm % Rem oval 2ppm 3ppm 100 4ppm 5ppm 95 90 0 20 40 60 80 100 T e m p e r a t u r e ( C ) Figure- 13: Effect of Temperature on Adsorption of SO 2 3.5 Adsorption isotherms 3.5.1 Langmuir adsorption isotherm The Langmuir adsorption isotherm is the best known linear model to determine the adsorption parameters. Langmuir model represented by following equation qe = KL Ce = Q0bCe 1+ bLCe 1+ bLCe The linearized form of Langmuir adsorption isotherm is as follows Ce = 1 + (1/Q0) Ce Q0bL Where qe is the amount adsorbed at equilibrium (mg/g), Q0 is the monolayer adsorption capacity (9mg/g), Ce the equilibrium concentration of adsorbate (mg/L) and bL is the Langmuir constant related to energy adsorption. The figure-14 shows the plot of Ce/qe against Ce. Values of Q0 and bL are in table-2. From the figure-14 and table-2 it was observed that the adsorption isotherm studies of removal of SO2 by silver nanoparticles does not fit for the Langmuir isotherm. 1 .1 0 0 C 40 C 1 .0 5 C e /q e 60 C 80 C 1 .0 0 0 .9 5 0 .9 0 0 2 4 6 Ce Figure-14: Langmuir adsorption plot for SO2 removal at different temperature 3.5.2 Freundlich adsorption isotherm The Freundlich equation is an empirical relationship describing the adsorption of solute from liquid to a solid surface. The Freundlich equation is expressed as qe = kf Ce1/n The linear form of Freundlich equation is as follows Log qe = log kf + 1/n (log Ce) www.ijera.com Where kf is the Freundlich adsorption capacity and n is the adsorption intensity. A plot of log q e versus log Ce gives a linear line with slope of 1/n and intercept of log kf given in table-2. From the figure-15 and table-2 it was observed that the adsorption of aqueous SO2 at different temperature perfectly fits in to Freundlich isotherm. The r2 value and ASS, values are more comparing to Langmuir isotherms. 69 | P a g e
  • 10. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 www.ijera.com 0 .8 0 C 40 C 0 .6 lo g q e 60 C 80 C 0 .4 0 .2 0 .0 0 .0 0 .2 0 .4 0 .6 0 .8 lo g C e Figure-15: Freundlich adsorption isotherm plots of SO2 removal at different temperature 3.5.3 Temkin adsorption isotherm 6 0 C 40 C 60 C 4 Ce 80 C 2 0 0 2 4 6 x /m Figure-16: Temkin adsorption isotherm plots of SO2 removal at different temperature. Temkin adsorption isotherm is studied by takes into account he interactions between adsorbents and metal ions to be adsorbed and is based on the assumption that the free energy of sorption is a function of the surface coverage [28]. The linear form of the Temkin isotherm is represented as: qe = B ln A + B ln Ce Where Ce is the equilibrium concentration of the adsorbate in mg/L, qe is the amount of adsorbate adsorbed at equilibrium (mg/g), RT/bT= B where T is the temperature (K) and R is the ideal gas constant (8.314 J mol-1K-1) and A and bT are constants. Figure16 showing relation between Ce and qe, from the figure-16 and table-2 it was observed that the adsorption of SO2 by silver nanoparticles is following Temkin adsorption isotherms. Table-1: Kinetic parameters for adsorption of Aqueous SO2 by Silver Nanoparticles S.No Parameters 01 R2 ASS K1 02 R2 ASS K2 03 R2 ASS α β www.ijera.com SO2concentration SO2 concentration (5 ppm/L) (10 ppm/L) Pseudo first order kinetic model 0.999 0.999 0.0 0.0 0.0625 0.0835 Pseudo Second order kinetic model 0.999 0.999 0.0505 0.0389 3.8196 X 10-3 10.2208 X 10-3 Elovich model 0.6788 0.6921 0.01285 0.1484 3.067 X 10-6 4.2026 X 10-6 92.2509 27.173 SO2 concentration (15 ppm/L) 0.8751 0.1062 0.1054 0.999 0.0167 5.4111 X 10-3 0.7867 0.3015 2.3743 X 10-6 19.033 70 | P a g e
  • 11. N. Gandhi et al Int. Journal of Engineering Research and Applications ISSN : 2248-9622, Vol. 4, Issue 1( Version 1), January 2014, pp.61-72 04 Intraparticle diffusion model 0.4286 0.02285 0.03969 0.008685 R2 ASS kid I www.ijera.com 0.4409 0.2695 0.1363 0.02982 0.5370 0.6546 0.2124 0.04648 Table-2: Isotherm kinetics for adsorption of Aqueous SO 2 by Silver Nanoparticles S.No Parameters 0 01 R2 ASS aT bT 0.999 0.0240 0.003618 0.001093 02 R2 ASS Q0 bL 0.05357 0.01071 0.002415 0.0007280 03 R2 ASS kf n 0.999 0.0147 0.001236 0.002558 IV. Temperature oC 40 60 Temkin Adsorption Isotherm 0.999 0.999 0.0240 0.0240 0.003618 0.003618 0.001093 0.001093 Langmuir Adsorption Isotherm 0.05357 0.05357 0.01071 0.01071 0.002415 0.002415 0.0007280 0.0007280 Freundlich Adsorption Isotherm 0.999 0.999 0.0147 0.0147 0.001236 0.001236 0.002558 0.002558 Conclusion In this study, silver nanoparticles are synthesized by Ficus Elastica using the alternative energy source of microwave irradiation. The AgNPs are highly stable AgNPs synthesized in the present study are capable of adsorbing SO2 molecules from aqueous solution and these AgNPs are inefficient in adsorbing NO2. The formation of silver nanoparticles is confirmed by SEM and spectrophotometrically. Investigation carried out on adsorption studies revealed that it is following Pseudo second order kinetics. Optimum dosage for 98% removal of SO2 is equal to ecofriendly nontoxic energy saving method is employed in the synthesis of nanoparticles. The present study gives a new direction for developing a catalytic tube for controlling air pollutant SO 2 caused by petrol-drove vehicles. V. Acknowledgement [2] [3] [4] [5] The authors are sincerely thankful to Mrs. Sujatha Gangadhar, registrar JNIAS for her constant encouragement and for financial support for completing this project. REFERENCES [1] C. Krishnaraj, E. G. Jagan, S. Rajasekar, P. Selvakumar P. T. Kalaichelvan, and N. Mohan, “Synthesis of silver nanoparticles using Acalypha indica leaf extracts and its antibacterial activity against water borne pathogens”. ELSEVIER International www.ijera.com [6] [7] 80 100 0.999 0.0240 0.003618 0.001093 0.999 0.0240 0.003618 0.001093 0.05357 0.01071 0.002415 0.0007280 0.05357 0.01071 0.002415 0.0007280 0.999 0.0147 0.001236 0.002558 0.999 0.0147 0.001236 0.002558 journal Colloids and Surfaces B: Biointerfaces. Vol.76, pp. 50–56, 2010. A. Leela, and V. Munusamy, “Tapping the unexploited plant resources for the synthesis of silver nanoparticles”. African Journal of Biotechnology Vol. 7, no. 17, pp.3162-3165, 2008. J. Y. Song, and S. K. Beom, “Rapid biological synthesis of silver nanoparticles using plant leaf extracts”. Bioprocess and Biosystems Engineering, Vol.32, no.1, pp.79-84, 2009. M. Shivashankar, and G. Sisodia, “Biosynthesis of silver nanoparticles obtained from plant extracts of Moringa oleifera”. International journal of Life sciences Biotechnology and Pharma research Vol. 1, no. 3, pp.65-70, 2012. Y. Y. Loo, B. W. Chieng, M. Nishibuchi, and S. Radu, “Synthesis of silver nanoparticles by using tea leaf extract from Camellia sinensis”. Dovepress International Journal of Nanomedicine, Vol. 6, no. 2, pp. 2-17, 2012. R. Geethalakshmi, and D.V.L. Sarada, Synthesis of plant-mediated silver nanoparticles using Trianthema decandra extract and evaluation of their anti microbial activities”. International Journal of Engineering Science and Technology. Vol. 2, no. 5, pp.970-975, 2010. M. Goldberg, C. Dan, R. Nancy, and L. France. 2010. Environmental Health 71 | P a g e
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