IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308
__________________________________________________________________________________________
IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 434
SYNTHESIS OF γ- ALUMINA BY SOLUTION COMBUSTION METHOD
USING MIXED FUEL APPROACH (UREA+GLYCINE FUEL)
Baburao N. Sherikar1
, Arun M .Umarji2
1
Materials Research Centre Indian Institute of Science Bangalore India
2
Department of Ceramic and Cement Technology P.D.A.College of Engineering Gulbarga India
shantbabu@gmail.com
Abstract
Nano crystalline γ-Alumina powders were synthesized by Solution Combustion reaction between aluminium nitrate as oxidizer and a
mixture of urea and glycine fuel as reducer. In this fuel mixture, urea was taken as stoichiometric fuel and glycine was added as
excess fuel to alter the exothermicity of redox reaction between aluminium nitrate and urea. The ratio of urea to glycine had been
optimized to obtain single phase gamma alumina. A Multi channel thermocouple setup was used to measure the flame temperatures to
study the nature of combustion of various fuel mixtures. The variation of adiabatic flame temperature was calculated theoretically for
different urea/glycine mixture ratios according to thermodynamic concept and correlated with the observed flame temperatures. These
powders were characterized by XRD, SEM, showing that the powders were composed of polycrystalline oxides with crystallite size of
81 nm for alpha alumina, ~ 5 nm for gamma alumina and having highly porous microstructure. An interpretation based on maximum
combustion temperature and the amount of gases produced during reaction for various urea to glycine ratio composition had been
proposed for the nature of combustion and its correlation with the characteristics of as synthesized powder.
Keywords: Nano crystalline materials, Gamma Alumina; Adiabatic flame temperature; Solution combustion route;
Urea+glycine mixture, Multi channel thermocouple setup, X-ray diffraction, Mixed fuel approach,
--------------------------------------------------------------------***---------------------------------------------------------------------
1. INTRODUCTION
Nanocrystalline (γ) alumina is a polytype of alumina that find
extensive applications as a catalyst and catalytic supports due
to its high surface area and porosity. These properties result
primarily from the nano-scale character of the alumina. Many
attempts have been made in literature to address the synthesis
of gamma alumina by using kaolin [1,2], boehmite sol [3],
saccharide molecule template [4] hydrothermal method [5,6] ,
precipitation method [7,8,9], sol-gel process [10,11], resin
synthesis method [12] , solvothermal route [13], reduction–
magnetic separation method [14]. But these methods are time
consuming, expensive and complex. Solution Combustion
Synthesis (SCS) provides simple, low cost fast process, with
energy and time saving to produce pure nano crystalline
ceramic powders [15]. (γ) alumina is synthesized by oxalyl
dihydrazide (ODH) fuel which is hydrazine hydrate derivative
and a carcinogenic. Except urea and glycine, most of the other
fuels (ODH, carbohydrazide etc) used in the SCS are
hydrazine derivatives. J.C .Toniolo et al [16] obtained
amorphous product during aluminum nitrate glycine
combustion with varying the oxidizer to fuel ratio. Only on
heating as prepared powder to 1073 K γ alumina phase is
formed.
Usage of mixed fuel approach to synthesis various ceramics
have been done earlier [17, 18, 19]. However, till now there is
no report of synthesis of gamma alumina by Solution
Combustion Synthesis using mixed fuel approach explaining
the thermodynamic concept. In this work effect of mixed fuel
approach using urea and glycine fuels on aluminiumnitrate
fuel combustion was investigated. Theoretical temperature and
enthalpy of reaction were calculated on thermodynamic
concept and correlated with the measured temperature. Urea to
glycine ratio was optimized to achieve pure gamma alumina
phase in as prepared state.
2. EXPERIMENTAL PROCEDURE
The reactants analytical grade aluminium nitrate
nonahydrate Al (NO3)3·9H2O was used as oxidizer. The
urea [CO(NH2)2] and glycine (C2H5NO2) were used as
fuel. The molar ratios/amount of reactants are shown in
Table1. The fuel mixture composition is designed such that
amount of fuel urea is taken according to stoichiometric
condition and kept constant for all composition and
glycine fuel was added as excess fuel to urea with wt
equivalent to 0, 10, 20, 30, 40wt% of urea, means for 3gm
of urea glycine was added as 0.0, 0.3, 0.6, 0.9, 1.2g
respectively. Totally five sample compositions were made
with notation, U00G, U10G, U20G, U30G, and U40G.
IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308
__________________________________________________________________________________________
IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 435
The Above compositions were dissolved in minimum
amount of deionized water to make clear solutions. These
solutions were then kept in furnace preheated to 773 K.
First thermal dehydration occured at ~ 373 K, at ~473 K
the viscous liquids swelled and auto ignited, with the rapid
evolution of large volume of gases. Here combustion
reaction takes place between decomposition products of
oxidizer and fuel leading to exothermic reaction giving
huge amount of energy in terms of heat and the local
temperature generated may be nearly 1773K which helps
in forming the ceramic oxide. The ash obtained after
releasing of gases was the desired ceramic product. Whole
reaction completes within a span of six to seven minutes.
The obtained product was highly porous due to huge
number of gases released during process .All combustion
calculations are mentioned in our earlier paper [20]. The
powder color varied with number of moles of glycine (Ψ).
At Ψ=0, it was white and changes to gray at Ψ=1.6. The
color change was due to residual carbon of incomplete
combustion. Under the equilibrium conditions the standard
reaction equation of systems can be represented for all
nitrate- Urea/glycine ratio combustion
3. THERMODYNAMIC MODELLING
As Solution Combustion Synthesis was fast and completed in
few seconds, it was be assumed as adiabatic. Temperature
generated due to the exothermic reaction was adiabatic
temperature. Using the thermodynamic data for the various
reactants and products listed in Table II, the enthalpy of
combustion and the theoretical adiabatic flame temperatures as
a function of urea/glycine ratio were approximately calculated
by the following equations using Mathematica software for
comparing exothermicity of combustion
ΔHo
= (∑nΔHo
) products-(∑nΔHo
) reactants (2)
( )
ad
3
To
ΔH = nC dT ( )p products298
∫
Table.1 Composition of reactants , Tad, Measured Temperature, Enthalpy of combustion, Nature of combustion
Sl.
No
Sampl
e code
Al(N
O)3
(g)
Urea
(g)
Glyci
ne (g)
Ψ Tad
(K)
Measu
red
Temp
(K)
ΔHO
(kcal/
mol)
Color Obtained
Powder /
1gm
desired
Nature of
combustion
1 U00G 7.5 3 0.00 0.
0
1390 1263 -375.21 White 0.940 Flaming
2 U10G 7.5 3 0.30 0.
4
1569 1143 -457.76 White 0.904 Flame + smoldering
3 U20G 7.5 3 0.60 0.
8
1733 1121 -540.31 grey 1.036 smoldering
4 U30G 7.5 3 0.90 1.
2
1882 1100 -622.85 grey 1.096 smoldering
5 U40 G 7.5 3 1.20 1.
6
2020 1081 -705.40 grey 1.130 smoldering
( ) 2
2 3 2 2 2
3 2 2 2 2 23
O (8 0.5 )N (5 2 )CO (28 2.5 )H O...(1)
2Al NO .9H O 5NH CONH + NH CH COOH+2.25 O
Al
Ψ Ψ →
+ + Ψ + + Ψ + + Ψ
+
IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308
__________________________________________________________________________________________
IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 436
Here ΔHo
is the enthalpy of combustion reaction, Cp is the
heat capacity of products at constant pressure and Tad is the
adiabatic flame temperature in Kelvin. Number of moles of
gases evolved per mole of product also calculated for all
reactions.
4. ENTHALPY OF COMBUSTION AND
ADIABATIC FLAME TEMPERATURE (TAD)
The ΔHo
and the Tad as function of urea/glycine ratio are
shown in Table.1. It was seen that ΔHo
, Tad and number of
moles of gases evolved were directly proportional to the
amount of glycine, varying linearly in ascending manner. The
variation can be expressed in linear equation as ΔH0
=375-206
Ψ, Tad=393 Ψ +1404K and number of moles of gases
evolved= 5Ψ +31. The reaction between urea and aluminum
nitrate at stoichiometric ratio for Ψ =0 mole of glycine had
lowest exothermicity and adiabatic flame temperature of
1390K. Adiabatic temperatures for Ψ= 0.4, 0.8, 1.2, 1.6 are
1569, 1733, 1880, 2020K, respectively. But measured flame
temperatures were very low and inversely proportional to the
number of moles of glycine. Low temperature might be due to
heat loss, heat capacity & thickness of thermocouple. But here
glycine plays major role instead of increasing it decreased the
combustion temperature due to its complexing ability, zwitter
ionic nature which might have formed the temporary complex
and might be decomposed later without forming the
hypergolic mixture of gases (HCNO+NOX+NH3 which were
necessary to form to give exothermic reaction releasing huge
energy) and also the high number of carbon atoms present in
glycine decrease the flame temperature due to zero value of
their enthalpy of formation. In spite of high reaction enthalpy
and Tad observed for all cases the crystalline phase had not
formed for Ψ=1.2,1.6 .This might be due to the strong
coordination compound formation in between the fuel glycine
and nitrate which prevented the release of the aluminium
cations to form compound.
5. PHASE FORMATION AND MORPHOLOGY
X-ray diffraction was carried on the combustion-synthesized
powders for phase identification scanned at a rate of 1°/min,
using Cu-K_ radiation on a Brukers D8 diffractometer, and the
crystallite size estimation was done using Scherrer formula
.Silicon was used as an external standard for correction due to
instrumental broadening. Microstructure studies on the
powders were carried out by using QUANTA 200 ESEM FEI.
Scanning electron microscope
Fig 1 shows XRD pattern of the as-synthesized powders of
different urea to glycine ratio. The formation of phase pure
crystalline α-alumina is confirmed for the case Ψ =0 as the
amount of glycine content increases the phase formation also
changes adding 0.4moles of glycine the phase changes from
pure alpha alumina to mixture of alpha and gamma alumina.
Finally it converts to completely to gamma alumina at addition
of 0.8 moles of glycine to the composition. U20G composition
shows the pure gamma alumina formation which is confirmed
by comparing the peaks with JCPDS Card No 29-0063, and
alpha alumina peaks were compared to the peaks of standard
JCPDS Card No 46-1212. Further increasing the glycine
content the phase changes to amorphous at 1.6 moles of
glycine .The change in phases from high temperature alpha
corundum phase to low temperature gamma phase and
amorphous phase even at high theoretical temperature and
enthalpy is due to incomplete combustion taking place due to
high number of carbon atoms present in glycine which leads to
the formation of carbon residue due to zero enthalpy of
formation and also glycine being complexing agent and
zwitter ionic nature leads to formation of temporary legand
complex formation which will have high decomposition
Table .2. Relevant thermodynamics data [21-22]
Compound Hf (kcal/ mol) Cp cal/(mol K)a
Al (NO3)3·9H2O (c) --857.59
NH2CONH2 -79.71
NH2CH2COOH(c) -126.22)
Al2O3 (c) -- 400.4 22.08 + 0.0089T
CO2 (g) -94.051 10.34 + 0.0027T
N2 (g) 0 6.5 + 0.0010T
H2O (g) -57.796 8.22+0.00015T
O2 (g) 0 8.27+0.000258T
IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308
__________________________________________________________________________________________
IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 437
temperature and prevent the formation of hypergolic gases. It
can be seen that crystallite size is highest Ψ =0 at
stoichiometric (81 nm) due to sintering of fine particles from
high local temperature, decreases as one moves to fuel rich
composition Ψ =0.4,0.8,1.2,1.6 due to low local temperature
preventing the sintering of particles . Fig.2(a) illustrates TEM
micrographs of SCS powder of stoichiometric alumina
showing an aggregate of crystallites of dimension 300 nm with
average crystallite size of 80-90 nm. Fig 2 (b), shows the SEM
micrographs of alumina powder of Ψ =0 of 400 μm and 300
μm, with porous structures respectively due to high and less
froth/gel formation in reactions. Fig. 2(c) shows the average
crystallite size of ~ 5 nm of γ-Alumina.
Fig. 1. XRD of alumina powders with varying Ψ.
Fig2 (a) TEM of U00G (b) SEM of U00G (c) TEM of U20G
CONCLUSIONS
A mixture-of-fuels approach has been employed to rapidly
synthesize single phase polycrystalline powders of γ-Alumina
using a mixture of urea and glycine as fuel in a solution-
combustion method. The ratio of urea to glycine has been
optimized to obtain single phase gamma alumina. For U20G
(Ψ =0.8) composition pure gamma alumina phase obtained.
The powder was nanocrystalline in nature with average
crystallite size of ~5 nm as confirmed by XRD and highly
porous as confirmed by SEM.
Theoretical adiabatic flame temperatures were calculated
according to the thermodynamic concept and compared with
the measured data. It was found that the theoretical adiabatic
temperature increased with increasing the value of glycine to a
maximum of 2020K (at Ψ = 1.6) but measured temperature for
the same was 1081K .This huge difference in temperature may
be due to more moles of gases formed during combustion take
away the heat generated and also due to incomplete
combustion occurred due to more no of carbon atoms present
in glycine. Glycine fuel reduces the exothermicity of
combustion reaction and acting as both complexing agent and
fuel.
10 20 30 40 50 60 70 80
ΨΨΨΨ=1.2
ΨΨΨΨ=1.6
ΨΨΨΨ=0.8
ΨΨΨΨ=0.4
U40G
U30G
U20G
γγγγγγγγ
γγγγ
γγγγ
αααα
αααααααα
αααα
αααα
αααααααα
αααα Alumina
*
Intensityina.u
2θ/θ/θ/θ/(degree)
U10G
αααα
γγγγ
Alumina
20 30 40 50 60 70 80
0
5000
10000
15000
20000
25000
30000
35000
40000
45000
Intensity
2θ/θ/θ/θ/((((deg)
U00G
IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308
__________________________________________________________________________________________
IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 438
REFERENCES
[1]. Huaming Yang , Mingzhu Liu, Jing Ouyang, Novel
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[3]. Qian Liu, Aiqin Wang, Xuehai Wang, Peng Gao,
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catalytic applications of mesoporous gamma alumina from
boehmite sol, Microporous and Mesoporous Materials,
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[4]. Benjing Xu , Jun Long, Huiping Tian, Yuxia Zhu, Xin
Sun, Synthesis and characterization of mesoporous gamma-
alumina templated by saccharide Molecules, Catalysis Today
147S (2009) S46–S50
[5]. Hyun Chul Lee, Hae Jin Kim, Chang Houn Rhee,
Synthesis of nanostructuredγ-alumina with a cationic
surfactant and controlled amounts of water Microporous and
Mesoporous Materials 79 (2005) 61–68
[6]. Ye Liu, Ding Ma, Xiuwen Han, Xinhe Bao, Wiebke
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Materials Letters,
Volume 62, Issue 8-9, 31, March 2008, pages 1297-1301
[7]. K.M. Parida, A.C.Pradhan, J.Das, Nruparaj Sahu
Synthesis and characterization of nano-sized porous gamma-
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and Physics Vol 113, Issue 1, 2009, Pages 244–248
[8]. H.S.Potdar, Ki-Won Jun, JongWook Bae, Seung-Moon
Kim ,Yun-JoLee, Synthesis of nano-sized porous γ-alumina
powder via a precipitation/digestion route, Applied Catalyst
A;General Volume 321,Issue2,11 April 2007,Pages 109-116
[9]. Shaoyan Wang,Xiaoan Li, Shaofeng Wang, Yang
Li,Yuchun Zhai Synthesis of γ-alumina via precipitation in
ethanol ,Materials Letters volume 62,Issue20,31,July 2008,
Pages 3552-3554
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[14]. Pengcheng Liu, Junting Feng, Xiangmei Zhang, Yanjun
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Synthesis of γ alumina by solution combustion method

  • 1. IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308 __________________________________________________________________________________________ IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 434 SYNTHESIS OF γ- ALUMINA BY SOLUTION COMBUSTION METHOD USING MIXED FUEL APPROACH (UREA+GLYCINE FUEL) Baburao N. Sherikar1 , Arun M .Umarji2 1 Materials Research Centre Indian Institute of Science Bangalore India 2 Department of Ceramic and Cement Technology P.D.A.College of Engineering Gulbarga India shantbabu@gmail.com Abstract Nano crystalline γ-Alumina powders were synthesized by Solution Combustion reaction between aluminium nitrate as oxidizer and a mixture of urea and glycine fuel as reducer. In this fuel mixture, urea was taken as stoichiometric fuel and glycine was added as excess fuel to alter the exothermicity of redox reaction between aluminium nitrate and urea. The ratio of urea to glycine had been optimized to obtain single phase gamma alumina. A Multi channel thermocouple setup was used to measure the flame temperatures to study the nature of combustion of various fuel mixtures. The variation of adiabatic flame temperature was calculated theoretically for different urea/glycine mixture ratios according to thermodynamic concept and correlated with the observed flame temperatures. These powders were characterized by XRD, SEM, showing that the powders were composed of polycrystalline oxides with crystallite size of 81 nm for alpha alumina, ~ 5 nm for gamma alumina and having highly porous microstructure. An interpretation based on maximum combustion temperature and the amount of gases produced during reaction for various urea to glycine ratio composition had been proposed for the nature of combustion and its correlation with the characteristics of as synthesized powder. Keywords: Nano crystalline materials, Gamma Alumina; Adiabatic flame temperature; Solution combustion route; Urea+glycine mixture, Multi channel thermocouple setup, X-ray diffraction, Mixed fuel approach, --------------------------------------------------------------------***--------------------------------------------------------------------- 1. INTRODUCTION Nanocrystalline (γ) alumina is a polytype of alumina that find extensive applications as a catalyst and catalytic supports due to its high surface area and porosity. These properties result primarily from the nano-scale character of the alumina. Many attempts have been made in literature to address the synthesis of gamma alumina by using kaolin [1,2], boehmite sol [3], saccharide molecule template [4] hydrothermal method [5,6] , precipitation method [7,8,9], sol-gel process [10,11], resin synthesis method [12] , solvothermal route [13], reduction– magnetic separation method [14]. But these methods are time consuming, expensive and complex. Solution Combustion Synthesis (SCS) provides simple, low cost fast process, with energy and time saving to produce pure nano crystalline ceramic powders [15]. (γ) alumina is synthesized by oxalyl dihydrazide (ODH) fuel which is hydrazine hydrate derivative and a carcinogenic. Except urea and glycine, most of the other fuels (ODH, carbohydrazide etc) used in the SCS are hydrazine derivatives. J.C .Toniolo et al [16] obtained amorphous product during aluminum nitrate glycine combustion with varying the oxidizer to fuel ratio. Only on heating as prepared powder to 1073 K γ alumina phase is formed. Usage of mixed fuel approach to synthesis various ceramics have been done earlier [17, 18, 19]. However, till now there is no report of synthesis of gamma alumina by Solution Combustion Synthesis using mixed fuel approach explaining the thermodynamic concept. In this work effect of mixed fuel approach using urea and glycine fuels on aluminiumnitrate fuel combustion was investigated. Theoretical temperature and enthalpy of reaction were calculated on thermodynamic concept and correlated with the measured temperature. Urea to glycine ratio was optimized to achieve pure gamma alumina phase in as prepared state. 2. EXPERIMENTAL PROCEDURE The reactants analytical grade aluminium nitrate nonahydrate Al (NO3)3·9H2O was used as oxidizer. The urea [CO(NH2)2] and glycine (C2H5NO2) were used as fuel. The molar ratios/amount of reactants are shown in Table1. The fuel mixture composition is designed such that amount of fuel urea is taken according to stoichiometric condition and kept constant for all composition and glycine fuel was added as excess fuel to urea with wt equivalent to 0, 10, 20, 30, 40wt% of urea, means for 3gm of urea glycine was added as 0.0, 0.3, 0.6, 0.9, 1.2g respectively. Totally five sample compositions were made with notation, U00G, U10G, U20G, U30G, and U40G.
  • 2. IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308 __________________________________________________________________________________________ IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 435 The Above compositions were dissolved in minimum amount of deionized water to make clear solutions. These solutions were then kept in furnace preheated to 773 K. First thermal dehydration occured at ~ 373 K, at ~473 K the viscous liquids swelled and auto ignited, with the rapid evolution of large volume of gases. Here combustion reaction takes place between decomposition products of oxidizer and fuel leading to exothermic reaction giving huge amount of energy in terms of heat and the local temperature generated may be nearly 1773K which helps in forming the ceramic oxide. The ash obtained after releasing of gases was the desired ceramic product. Whole reaction completes within a span of six to seven minutes. The obtained product was highly porous due to huge number of gases released during process .All combustion calculations are mentioned in our earlier paper [20]. The powder color varied with number of moles of glycine (Ψ). At Ψ=0, it was white and changes to gray at Ψ=1.6. The color change was due to residual carbon of incomplete combustion. Under the equilibrium conditions the standard reaction equation of systems can be represented for all nitrate- Urea/glycine ratio combustion 3. THERMODYNAMIC MODELLING As Solution Combustion Synthesis was fast and completed in few seconds, it was be assumed as adiabatic. Temperature generated due to the exothermic reaction was adiabatic temperature. Using the thermodynamic data for the various reactants and products listed in Table II, the enthalpy of combustion and the theoretical adiabatic flame temperatures as a function of urea/glycine ratio were approximately calculated by the following equations using Mathematica software for comparing exothermicity of combustion ΔHo = (∑nΔHo ) products-(∑nΔHo ) reactants (2) ( ) ad 3 To ΔH = nC dT ( )p products298 ∫ Table.1 Composition of reactants , Tad, Measured Temperature, Enthalpy of combustion, Nature of combustion Sl. No Sampl e code Al(N O)3 (g) Urea (g) Glyci ne (g) Ψ Tad (K) Measu red Temp (K) ΔHO (kcal/ mol) Color Obtained Powder / 1gm desired Nature of combustion 1 U00G 7.5 3 0.00 0. 0 1390 1263 -375.21 White 0.940 Flaming 2 U10G 7.5 3 0.30 0. 4 1569 1143 -457.76 White 0.904 Flame + smoldering 3 U20G 7.5 3 0.60 0. 8 1733 1121 -540.31 grey 1.036 smoldering 4 U30G 7.5 3 0.90 1. 2 1882 1100 -622.85 grey 1.096 smoldering 5 U40 G 7.5 3 1.20 1. 6 2020 1081 -705.40 grey 1.130 smoldering ( ) 2 2 3 2 2 2 3 2 2 2 2 23 O (8 0.5 )N (5 2 )CO (28 2.5 )H O...(1) 2Al NO .9H O 5NH CONH + NH CH COOH+2.25 O Al Ψ Ψ → + + Ψ + + Ψ + + Ψ +
  • 3. IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308 __________________________________________________________________________________________ IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 436 Here ΔHo is the enthalpy of combustion reaction, Cp is the heat capacity of products at constant pressure and Tad is the adiabatic flame temperature in Kelvin. Number of moles of gases evolved per mole of product also calculated for all reactions. 4. ENTHALPY OF COMBUSTION AND ADIABATIC FLAME TEMPERATURE (TAD) The ΔHo and the Tad as function of urea/glycine ratio are shown in Table.1. It was seen that ΔHo , Tad and number of moles of gases evolved were directly proportional to the amount of glycine, varying linearly in ascending manner. The variation can be expressed in linear equation as ΔH0 =375-206 Ψ, Tad=393 Ψ +1404K and number of moles of gases evolved= 5Ψ +31. The reaction between urea and aluminum nitrate at stoichiometric ratio for Ψ =0 mole of glycine had lowest exothermicity and adiabatic flame temperature of 1390K. Adiabatic temperatures for Ψ= 0.4, 0.8, 1.2, 1.6 are 1569, 1733, 1880, 2020K, respectively. But measured flame temperatures were very low and inversely proportional to the number of moles of glycine. Low temperature might be due to heat loss, heat capacity & thickness of thermocouple. But here glycine plays major role instead of increasing it decreased the combustion temperature due to its complexing ability, zwitter ionic nature which might have formed the temporary complex and might be decomposed later without forming the hypergolic mixture of gases (HCNO+NOX+NH3 which were necessary to form to give exothermic reaction releasing huge energy) and also the high number of carbon atoms present in glycine decrease the flame temperature due to zero value of their enthalpy of formation. In spite of high reaction enthalpy and Tad observed for all cases the crystalline phase had not formed for Ψ=1.2,1.6 .This might be due to the strong coordination compound formation in between the fuel glycine and nitrate which prevented the release of the aluminium cations to form compound. 5. PHASE FORMATION AND MORPHOLOGY X-ray diffraction was carried on the combustion-synthesized powders for phase identification scanned at a rate of 1°/min, using Cu-K_ radiation on a Brukers D8 diffractometer, and the crystallite size estimation was done using Scherrer formula .Silicon was used as an external standard for correction due to instrumental broadening. Microstructure studies on the powders were carried out by using QUANTA 200 ESEM FEI. Scanning electron microscope Fig 1 shows XRD pattern of the as-synthesized powders of different urea to glycine ratio. The formation of phase pure crystalline α-alumina is confirmed for the case Ψ =0 as the amount of glycine content increases the phase formation also changes adding 0.4moles of glycine the phase changes from pure alpha alumina to mixture of alpha and gamma alumina. Finally it converts to completely to gamma alumina at addition of 0.8 moles of glycine to the composition. U20G composition shows the pure gamma alumina formation which is confirmed by comparing the peaks with JCPDS Card No 29-0063, and alpha alumina peaks were compared to the peaks of standard JCPDS Card No 46-1212. Further increasing the glycine content the phase changes to amorphous at 1.6 moles of glycine .The change in phases from high temperature alpha corundum phase to low temperature gamma phase and amorphous phase even at high theoretical temperature and enthalpy is due to incomplete combustion taking place due to high number of carbon atoms present in glycine which leads to the formation of carbon residue due to zero enthalpy of formation and also glycine being complexing agent and zwitter ionic nature leads to formation of temporary legand complex formation which will have high decomposition Table .2. Relevant thermodynamics data [21-22] Compound Hf (kcal/ mol) Cp cal/(mol K)a Al (NO3)3·9H2O (c) --857.59 NH2CONH2 -79.71 NH2CH2COOH(c) -126.22) Al2O3 (c) -- 400.4 22.08 + 0.0089T CO2 (g) -94.051 10.34 + 0.0027T N2 (g) 0 6.5 + 0.0010T H2O (g) -57.796 8.22+0.00015T O2 (g) 0 8.27+0.000258T
  • 4. IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308 __________________________________________________________________________________________ IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 437 temperature and prevent the formation of hypergolic gases. It can be seen that crystallite size is highest Ψ =0 at stoichiometric (81 nm) due to sintering of fine particles from high local temperature, decreases as one moves to fuel rich composition Ψ =0.4,0.8,1.2,1.6 due to low local temperature preventing the sintering of particles . Fig.2(a) illustrates TEM micrographs of SCS powder of stoichiometric alumina showing an aggregate of crystallites of dimension 300 nm with average crystallite size of 80-90 nm. Fig 2 (b), shows the SEM micrographs of alumina powder of Ψ =0 of 400 μm and 300 μm, with porous structures respectively due to high and less froth/gel formation in reactions. Fig. 2(c) shows the average crystallite size of ~ 5 nm of γ-Alumina. Fig. 1. XRD of alumina powders with varying Ψ. Fig2 (a) TEM of U00G (b) SEM of U00G (c) TEM of U20G CONCLUSIONS A mixture-of-fuels approach has been employed to rapidly synthesize single phase polycrystalline powders of γ-Alumina using a mixture of urea and glycine as fuel in a solution- combustion method. The ratio of urea to glycine has been optimized to obtain single phase gamma alumina. For U20G (Ψ =0.8) composition pure gamma alumina phase obtained. The powder was nanocrystalline in nature with average crystallite size of ~5 nm as confirmed by XRD and highly porous as confirmed by SEM. Theoretical adiabatic flame temperatures were calculated according to the thermodynamic concept and compared with the measured data. It was found that the theoretical adiabatic temperature increased with increasing the value of glycine to a maximum of 2020K (at Ψ = 1.6) but measured temperature for the same was 1081K .This huge difference in temperature may be due to more moles of gases formed during combustion take away the heat generated and also due to incomplete combustion occurred due to more no of carbon atoms present in glycine. Glycine fuel reduces the exothermicity of combustion reaction and acting as both complexing agent and fuel. 10 20 30 40 50 60 70 80 ΨΨΨΨ=1.2 ΨΨΨΨ=1.6 ΨΨΨΨ=0.8 ΨΨΨΨ=0.4 U40G U30G U20G γγγγγγγγ γγγγ γγγγ αααα αααααααα αααα αααα αααααααα αααα Alumina * Intensityina.u 2θ/θ/θ/θ/(degree) U10G αααα γγγγ Alumina 20 30 40 50 60 70 80 0 5000 10000 15000 20000 25000 30000 35000 40000 45000 Intensity 2θ/θ/θ/θ/((((deg) U00G
  • 5. IJRET: International Journal of Research in Engineering and Technology eISSN: 2319-1163 | pISSN: 2321-7308 __________________________________________________________________________________________ IC-RICE Conference Issue | Nov-2013, Available @ http://www.ijret.org 438 REFERENCES [1]. Huaming Yang , Mingzhu Liu, Jing Ouyang, Novel synthesis and characterization of nanosized γ-Al2O3 from kaolin , Applied Clay Science 47 (2010) 438-443 [2]. Seyed Ali Hosseini, Aligholi Niaei, Dariush Salari ,Production of γ- Al2O3 from Kaolin ,Open Journal of Physical Chemistry, 2011, 1, 23-27 [3]. Qian Liu, Aiqin Wang, Xuehai Wang, Peng Gao, Xiaodong Wang, Tao Zhang, Synthesis ,characterization and catalytic applications of mesoporous gamma alumina from boehmite sol, Microporous and Mesoporous Materials, Volume 111, Issues 1–3, 15 April 2008, Pages 323-333 [4]. Benjing Xu , Jun Long, Huiping Tian, Yuxia Zhu, Xin Sun, Synthesis and characterization of mesoporous gamma- alumina templated by saccharide Molecules, Catalysis Today 147S (2009) S46–S50 [5]. Hyun Chul Lee, Hae Jin Kim, Chang Houn Rhee, Synthesis of nanostructuredγ-alumina with a cationic surfactant and controlled amounts of water Microporous and Mesoporous Materials 79 (2005) 61–68 [6]. Ye Liu, Ding Ma, Xiuwen Han, Xinhe Bao, Wiebke Frandsen, Di Wang, Dangsheng Su, Hydrothermal synthesis of microscale boehmite and gamma nanoleaves alumina, Materials Letters, Volume 62, Issue 8-9, 31, March 2008, pages 1297-1301 [7]. K.M. Parida, A.C.Pradhan, J.Das, Nruparaj Sahu Synthesis and characterization of nano-sized porous gamma- alumina by control precipitation method Materials Chemistry and Physics Vol 113, Issue 1, 2009, Pages 244–248 [8]. H.S.Potdar, Ki-Won Jun, JongWook Bae, Seung-Moon Kim ,Yun-JoLee, Synthesis of nano-sized porous γ-alumina powder via a precipitation/digestion route, Applied Catalyst A;General Volume 321,Issue2,11 April 2007,Pages 109-116 [9]. Shaoyan Wang,Xiaoan Li, Shaofeng Wang, Yang Li,Yuchun Zhai Synthesis of γ-alumina via precipitation in ethanol ,Materials Letters volume 62,Issue20,31,July 2008, Pages 3552-3554 [10]. Genoveva Buelna, Y.S. Lin,Sol–gel-derived mesoporous c-alumina granules, Microporous and Mesoporous Materials 30 (1999) 359–369 [11].Abbas Khaleel, Shamsa Al-Mansouri Meso-macroporous γ alumina by template-free sol-gel synthesis; The effect of the solvent and acid catalyst on the microstructure and texture properties Colloids and Surfaces A; Physicochemical and Engineering Aspects, volume 369,Issues 1-3,20 october 2010 pages 272- 280 [12]. D.M. Ibrahima, Y.M. Abu-Ayanab, Preparation of nano alumina via resin synthesis, Materials Chemistry and Physics 113 (2009) 579–586 [13]. Ming-Guo Ma , Jie-Fang Zhu , A facile solvothermal route to synthesis of γ-alumina with bundle-like and flower- like morphologies, Materials Letters 63 (2009) 881–883 [14]. Pengcheng Liu, Junting Feng, Xiangmei Zhang, Yanjun Lin, David G. Evans, Dianqing Li,Preparation of high purity spherical g-alumina using a reduction-magnetic separation process Journal of Physics and Chemistry of Solids 69 (2008) 799–804 [15]. K C, Patil ,M.S Hegde,T. Rattan, S.T.Aruna Chemistry of nanocrystalline oxide materials; combustion synthesis, properties Sinapore;World Scientific;2008. [16]. J.C. Toniolo, M.D. Lima, Takimi, A.S., and Bergmann, C.P Synthesis of alumina powders by the glycine–nitrate combustion process Materials. Research. Buletein.,2005, vol. 40, pp. 561–571. [17]. S.T. Arunaa, N.S. Kinib, Satish Shetty, K.S. Rajama Synthesis of nanocrystalline CeAlO3 by solution-combustion route Materials Chemistry and Physics 119 (2010) 485–489 [18]. S. Banerjee, P. Sujatha Devi Sinter-active nanocrystalline CeO2 powder prepared by a mixed fuel process: Effect of fuel on particle agglomeration Journal of Nanoparticle Research (2007) 9:1097–1107 [19]. S.K. Ghosh, A. Prakash, S. Datta, S.K Roy, D.Basu Effect of fuel characteristics on synthesis of calcium hydroxyapatite by solution combustion route Bulletin of Materials Science, Vol. 33, 2010, pp. 7–16 [20]. Baburao Sherikar N,Umarji A M, Effect of adiabatic flame temperature on nano alumina powders during solution combustion process Transactions of Indian Ceramic Society. 70(3) 167-172(2011) [21]. R.H. Perry, C.H. Chilton, Chemical Engineering Handbook, 7th edn. (McGraw-Hill, New York, 1997). [22]. D. R.Lide, CRC Handbook of Chemistry and Physics 72nd edn. (CRC Press ,Boston 1991-1992).