1.embedded based system for the study of heats of mixing of binary liquid mixtures

International Journal of Current Research In Science, Engineering and Technology (IJCRSET)
Volume 1, Issue 4, August 2016, PP 01-12
www.ijcrset.com
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Embedded Based System For The Study Of Heats Of Mixing Of
Binary Liquid Mixtures
P.S.S Sushama1
, K.Malakondaiah 2
, C.Nagaraja3
123
(Department of Instrumentation and USIC, SKDU, Ananthapur, India)
______________________________________________________________________________________
Abstract : Studies of heats of reactions of binary liquid mixtures are given a considerable importance in
understanding the nature of molecular interactions. Such studies mainly help to know the enthalpies of liquid
mixtures. The present study deals with design of a simple embedded based system for measuring heat of mixing
of binary liquid mixtures. The system consists of two units, cell assembly and data acquisition system. One of the
components of the binary mixture is taken into the cell, other component is injected in to the cell through
appropriate mechanical arrangement. The reaction on mixing causes the thermal changes which are sensed by
the thermal sensor, that can be measured up to 10-4o
C. The entire unit is interfaced to LPC 2366 ARM based
controller (A less power consumption device made by philips). The ARM controller sends the data to the
Personal Computer through the serial port and software is developed to calculate enthalpy values. A
comparison of the results obtained with the literature data showed good agreement. The designed system can be
used as an alternative for the measuring heats of mixing of binary liquid mixtures. The paper deals with the
design aspects both hardware and software features of the system.
_______________________________________________________________________________________
Keywords - liquids, mixtures, ARM Processor, embedded
I. INTRODUCTION
Heat of mixing data for binary liquid systems is useful for both chemists and engineers to know the
nature of the solutions and design the heat transfer equipment (heat exchangers). As the data of the non ideal
systems are very limited and the effect of temperature are very rarely has been investigated. Based on heat
transfer theory, the relations between the heat effect generated and the quantity measured in the calorimeter
known as the heat balance equation is established, which expresses the change of temperature directly as a
function of the heat produced in a calorimeter and is applied to design different types of calorimeters. A number
of calorimeter is available micro to macro and simple to complex in design. The calorimeters are differed by
their principle, heat flow calorimeter, Benson et. al.1
Picker flow calorimeter, Fortier and Benson2
in this type
of calorimeter excess heat capacities of mixtures of non-electrolytes were determined from volumetric heat
capacity. Steady state and composition scanning differential flow micro calorimeters by Patrick Picker et. al.3,4
They developed two different flow micro calorimeters, one is of the adiabatic type and can be used to
measure ΔT mixing for liquid phase reactions, and other can be operated under either adiabatic or isothermal
conditions and serves for either gas or liquid phase investigations. The available commercial calorimeters like
Parr5,6
and ITC are sophisticated and very costly. Hence an attempt is made to design adiabatic micro
calorimeter which is simpler and versatile for a rapid and fairly accurate measurement of exothermic and
endothermic heats of mixing for binary liquid mixtures. The proposed system shows a new approach which is
attached with all the advantages of any embedded based system in speed and compatibility. These
measurements assume a great significance because of diversified applications of these measurements in
industries and R&D purposes.
II. MATERIALS AND METHODS
The chemicals used in the present work Carbon tetrachloride, n-hexane, Cyclohexane , Dimehyl
formamide, methyl-tert-butylethane (MTBE), Chlorobenzene, Nitrobenzene, Carbontettachloride are obtained
from M/s Fulka Ltd.,Bombay. Benzene (Spectroscopic grade) was obtained from M/s SD Fine Chemicals,
Boisar, India. Dimethoxyethane are obtained from SD Fine Chemicals, Boisar, India The chemicals used here
are used without any further purification. methyl-isobutyl ketone, methyl-ethylketone obtained from BDH Ltd.,
and dried over 4A molecular sieves for 4 – 5 days and purified by fractional distillation. Pure component
properties used to calculate excess enthalpies such as molecular weight, density and heat capacity are collected
and tabulated in Table 1. Measured density, boiling point and refractive index of the the compounds and
compared with literature values reported by Riddick et al7
and Ian M. Smallwood8
to ensure the purity of the
compounds. The data is tabulated in Table2. From Table2, it is found that the measured properties are in good
agreement with literature values9,10
. The purity of the compounds are checked and further confirmed by GC, a

International Journal of Current Research In Science, Engineering and Technology
single sharp peak. The vibrator, Nokia 1100 (range is 500 milli volts to one volt) is used as a device to stir the
mixture inside the cell, the ARM7TDMI based LPC2366 controller (NXP Philips), 12V and 2Amp stepper
motor similar to that used in HP printer, constant current source REF200 and 5 k thermistor are purchased
from local electronic shop, Ahmedabad, India. Micro syringe (Borosil) of 10 ml capacity, Dewar flask (Eagle)
of 20 ml capacity are obtained from Ahmedabad, India. Insulating materials is Polytherific foam (PUF) from
M/s Bharathi Refrigeration systems from Ahmedabad, India.
The heats of mixing is calculated using the equation.
Where T temperature difference, w is weight and CP is heat capacity of the components, C.C is cell
constant. Suffixes represent components 1 and 2 respectively. The pure component data is collected from
literature is tabulated in Table2.
Table 1 Properties of pure components from literature value
Table 2 Comparison of properties of pure components
Sl.
No.
Name of
the
compoun
d
Mole
cular
weig
ht
Density
g/cc
Cp,
Cal/
mol/o
C
Chemical
Formula
Re
fer
en
ces
1 DMF 73 0.945 36 C4H10O2 5
2 MIBK 100 0.801 46 C6H12O
3 MEK 72 0.805 38 C4H10O
4 MTBE 88 0.741 44.8 C5H12O
5 Benzen
e
78 0.790 31 C6H6
6 Chloro
Benzen
e
113 1.106 35 C4H5cl
7 Nitro
benzen
e
123 1.204 44 C6H5NO2
8 Hexane 86 0.659 42.0 C6H14
9 Cyclo
hexane
84 0.778 36.4 C6H12
10 Ethanol 46 0.789 27 C6H5O
11 Water 18 0.998 18 H2O
12 Carbon
tetrachl
oride
154 1.580 32 CCl4
Sl.
N
o.
Name of
the
compoun
d
Density g/cc Boiling point,
o
C
Refractive Index Ref.
Expt. Lit. Expt. Lit. Expt. Lit.
1 DMF 0.9453 0.945 152.6 153 1.4276 1.427 5
2 MIBK 0.8007 0.801 116.3 116 1.3945 1.394
3 MEK 0.8039 0.805 79.8 80 1.3772 1.377
4 MTBE 0.7402 0.741 55.2 55 1.3686 1.369
5 Benzene 0.7896 0.790 79.8 80 1.4978 1.498
6 ChloroBe
nzene
1.1062 1.106 131.7 132 1.5236 1.523
7 Nitro
benzene
1.2038 1.204 210.8 211 1.5488 1.550
8 Hexane 0.6578 0.659 69.4 69 1.3725 1.372
9 Cyclo
hexane
0.7782 0.778 80.6 81 1.4242 1.424
10 Ethanol 0.7886 0.789 78.2 78 1.3586 1.359
11 Water 0.9982 0.998 99.8 100 1.3323 1.332
12 Carbon
tetrachlor
ide
1.5796 1.580 75.6 76 1.4592 1.459
 CCCwCwTH PP
E
.2211 

III. APPARATUS
The calorimeter was designed to operate adiabatically and to allow the heats of mixing at room
temperature to determine for the entire composition range. The designed system consists of two units. One is
calorimeter cell assembly and other is data acquisition system. The Cell design is as shown in fig.1.
The cell assembly consists of a test cell of 10 ml capacity inserted in a Dewar flask, which is insulated
with Polytherific foam material about 2 mm thickness. One of the components of binary mixture is taken into
the test cell and other component is added by means of dispensing unit. The dispensing unit consist of 12 V
stepper motor, gear rod, coupling and micro syringe. Syringe is taken and attached to a gear rod. Stepper motor
is plugged to a 12 V power supply and interfaced to LPC 2366 ARM controller. The syringe is connected to a
feed tube at one end and the other end is kept in to the cell inside Dewar flask. A 5 k thermistor was taken.
The thermistor is a glass covered probe with a resistance of 5 k at room temperature was sealed in the end of a
piece of glass tubing which carried the leads a out of the calorimeter. One of the lead is connected to constant
current source REF200 and the other lead is grounded to the power supply. The thermistor is inserted in the
solution. Thermistor senses the temperature changes produced on adding second component to the other
component which was held in the calorimeter cell. The sensed voltages are sent to the ADC channle2 of the port
pin 24 of ADC of LPC 2366 ARM controller and data is acquired from the PC through the serial port .A tiny
DC motor is taken and the leads are taken out and plugged to 900 mV power supply. A small glass tube is taken
and bended at the edge to act this as a stirrer. The glass tube is fixed to the tip of the motor. Stirrer runs at a very
low speed, so that the heat produced due to the stirrer is negligible. Here the designed tiny stirrer will not
produce any frictional heat while stirring.
Fig 1 Calorimeter Design
IV. EXPERIMENTAL PROCEDURE
The designed specification of calorimeter used for the measurement of heat of mixing for binary liquid
mixtures is as shown in Fig.1. First data point is obtained by taking known quantity (5 ml) of component 1 into
test cell and the 0.5 ml of component 2 is added through dispensing unit. A Vibrator is used to provide uniform
distribution of the component 2 into component 1 in the cell. The temperature change is recorded at every 5
seconds. Experiment is stopped after reaching thermal equilibrium, i.e., no temperature change. 0.5 ml of
component 2 is added to the mixture (5.5 ml) in the cell. The temperature change is recorded at every 5 seconds
and stopped after reaching thermal equilibrium. The procedure is repeated till total amount of component 2
added is 5 ml with a 0.5 ml increment. . The temperature difference (T) is obtained by plotting time vs.
temperature. Up to 50% weight percent range is covered in this way. To obtain the data over entire composition

range, the procedure is repeated by interchanging components 2 and 1, by taking 5 ml of component 2 in the cell
and added component 1 in the increments of 0.5 ml.
V. RESULTS AND DISCUSSIONS
The designed calorimeter is tested with a number of binary systems.
Table 3A Determination of cell constants using Cyclo Hexane + n-Hexane system
Table 3B Determination of cell constants using Benzene + CCl4 system
No adiabatic calorimeter is fully adiabatic, some heat will be lost by the sample to the sample holder. A
mathematical correction factor, known as the cell constant, can be used to adjust the calorimetric result to
account for these heat losses. Every calorimeter has a unique calorimeter constant. It may be calculated by
applying a known amount of heat to the calorimeter and measuring the calorimeter's corresponding change
in temperature. The calorimeter constant is then calculated by dividing the change in enthalpy (ΔH) by the
change in temperature (ΔT). In our study we have determined calorimeter constant from the experiment results
with the literature values for two different binary systems, cyclo alkane and normal chain alkane system, i.e.,
Mole
fraction
Temp
diff HE
, ca/g
Cell
const.
X1 DT Expt Lit Diff Diff/ DT
0.1085 -0.0988 0.1988 2.3047 2.1060 21.3199
0.1958 -0.0589 0.1139 1.3839 1.2700 21.5664
0.2675 -0.0714 0.1501 1.6880 1.5380 21.5415
0.3275 -0.0964 0.2188 2.2971 2.0782 21.5661
0.3784 -0.1207 0.2945 2.8867 2.5922 21.4734
0.4221 -0.1389 0.3625 3.3584 2.9959 21.5644
0.4601 -0.1519 0.4221 3.6979 3.2758 21.5635
0.4934 -0.1599 0.4715 3.9204 3.4489 21.5625
0.5228 -0.1643 0.5122 4.0481 3.5359 21.5178
0.5490 -0.1642 0.5396 4.1030 3.5634 21.7014
0.5490 -0.1640 0.5613 4.1030 3.5417 21.5956
0.5750 -0.1661 0.5402 4.1010 3.5608 21.4378
0.6035 -0.1645 0.5071 4.0346 3.5275 21.4452
0.6349 -0.1597 0.4650 3.8862 3.4212 21.4257
0.6699 -0.1503 0.4120 3.6385 3.2264 21.4673
0.7089 -0.1363 0.3503 3.2776 2.9273 21.4791
0.7527 -0.1171 0.2812 2.8032 2.5220 21.5304
0.8023 -0.0959 0.2138 2.2488 2.0350 21.2275
0.8589 -0.0738 0.1529 1.7249 1.5720 21.3011
0.9241 -0.0656 0.1209 1.5116 1.3907 21.2090
429.4956
Average Value 21.4748
mole
fraction temp dif Qmix , cal/g Diff Diff/DT
X1 DT Expt. Lit.
0.9080 -0.0237 0.0411 0.554664 -0.51356 21.66934
0.8315 -0.0426 0.080877 0.995101 -0.91422 21.46067
0.7669 -0.0576 0.118819 1.356356 -1.23754 21.48502
0.7116 -0.0698 0.155455 1.659999 -1.50454 21.55507
0.6638 -0.0810 0.193709 1.920077 -1.72637 21.31319
0.6220 -0.0897 0.229178 2.146178 -1.917 21.37839
0.5851 -0.0974 0.264939 2.345107 -2.08017 21.35696
0.5524 -0.1036 0.298827 2.521859 -2.22303 21.45784
0.5231 -0.1095 0.333726 2.680204 -2.34648 21.43627
0.4968 -0.1142 0.366933 2.823053 -2.45612 21.50718
0.0898 -0.0221 0.039784 0.518298 -0.47851 21.65221
0.1649 -0.0404 0.07907 0.943367 -0.8643 21.39349
0.2285 -0.0560 0.118393 1.300488 -1.18209 21.10883
0.2831 -0.0680 0.154438 1.606293 -1.45185 21.35081
0.3305 -0.0792 0.192308 1.872179 -1.67987 21.21049
0.3720 -0.0880 0.227491 2.106235 -1.87874 21.34937
0.4086 -0.0950 0.2605 2.314384 -2.05388 21.61982
0.4413 -0.1020 0.295708 2.501076 -2.20537 21.62126
0.4705 -0.1099 0.335864 2.669737 -2.33387 21.23633
0.4968 -0.1106 0.355366 2.823053 -2.46769 22.31182
429.4744
Average value 21.4772

cyclohexane + n-Hexane and aromatic and chlorinated alkanes, i.e., Benzene + Carbontetrachloride (CCl4)11
.
Average value of the differences between experimental and literature values over the entire composition range
was taken as the cell constant. It was found that the cell constant for both the systems is similar. The results are
tabulated in Table 3A and Table 3B. The detailed calculation procedure is given in Appendix A.
The recorded temperature values are smoothened for finding the temperature difference (ΔT) values and the
enthalpy calculations done by using the C++ program.
Appendix A
Steps to calculate the cell constant
The pure component data, molecular weight, heat capacity and density are collected from the literature.
Cyclohexane (1) + n-Hexane (2)
Component Molecular weight Heat capacity Density (g/cc)
(cal/g. K)
Cyclohexane 84.61 0.43251 0.7785
n-Hexane 86.18 0.48735 0.6548
First Data Point
Weight of 5 ml of component 1 (w1) = 5 x 0.7785 = 3.8925 g
Weight of 0.5 ml of component 2 (w2)= 0.5x 0.6548 = 0.3274 g
Weight fraction = w1/(w1+w2)
= 3.8925/(3.8925+0.3274)= 0.9224
Mole fracton of component 1,
 2
2
1
1
1
1
1
MW
w
MW
w
MW
w
X

 =
 18.86
3274.0
611.84
8925.3
611.84
8925.3

= 0.9241
Average molecular weight = x1*MW1 + (1-X1)*MW2
= 0.9241x84.61 + (1-0.9241)*86.18
= 84.3133
Totals Moles in the mixture = Moles of component 1 (n1) + Moles of component 2 (n2)
= w1/MW! + w2/MW2
= 3.8925/84.61 + 0.3274/86.18
= 0.0501
Q1 = 0.0
Q2, (cal/g k) = -T(w1cp1 + w2cp2) T
Q2 = -( -0.0656(3.8925  0.43251 + 0.3274  0.48735))
= 0.1209
QMixt = Q1 + Q2 = 0 + 0.1190 = 0.1190 Cal/g K
Qmix, (Lit value)= 1.5116
Difference = Qmix, (Expt) - Qmix(Lit)
= 0.1209 - 1.5116
= - 1.3907Cell Constant = Difference / T
= - 1.3907/(-0.0656)
= 21.2090
Second Data Point
Weight of 5.5 ml mixture = 3.8925 + 0.3274 = 4.2199 g
Weight of 0.5 ml component2 = 0.3274 g
Step wise calculation of weight of each component in the mixture:
Step 1: weight of mixture x weight fraction of component 1/average molecular weight of mixture (as in data
point 1)
Weight of component 1 = 4.2199 x 0.9224 = 3.8925 g
Weight of component 2 in the mixture= 4.2199 x (1-0.9224) = 0.3274 8
Total weight of component 2 for second point = weight in the mixture and added weight
= 0.3274 +0 .3274 = 0.6548 g
Weight fraction = 3.8925/(3.8925 + 0.6548)
= 0.8560
Mole fraction = 3.8925/84.16 +0.6548/86.18 = 0.8589

Average molecular weight = 0.8589 x 84.61 + (1-0.8589) x 86.18 = 84.4450
Total moles = 3.8925/84.61 + 0.6548/86.18 = 0.0538
Q1 is the heat of mixing
Q1 = QMixt of data point 1 x weight fraction of component1/average molecular weight
Q1 = 0.1209 x 0.9224/84.3133
= 0.0051
Q2, (cal/g k) = -T(w1cp1 + w2cp2 )
= - (-0.0738 x (3.8925 x 0.43251 + 0.3274 x 0.48735))
= 0.1478
Qmix = 0.0051 + 0.1478 = 0.1529 cal/g K
= 0.1529 - 1.7249 = - 1.5720
Cell Constant = Difference / T
= - 1.5720/(-0.0738)
= 21.301
Third Data Point
Weight of mixture (6ml) = 4.2199 + 0.3274 = 4.5473 g
Weight of component 1 in the mixture = 4.5473 x 0.8560 = 3.8925
Weight of component 2 in the mixture = 4.5473 x (1-0.8560) = 0.6548
= 0.6548 + 0.3274 = 0.9822 g
Weight fraction = 3.8925/(3.8925 + 0.9822)
= 0.7985
Mole fraction = 3.8925/84.16 +0.9822/86.18 = 0. 8023
Average molecular weight = 0.7985 x 84.61 + (1-0.7985) x 86.18) = 84.5594
Total moles = 3.8925/84.61 + 0.9822/86.18 = 0.0576
Q1 = 1.529 x 0.8560/84.4450
= 0.065
Q2, (cal/g k) = -T(w1cp1 + w2cp2 + E)
= -(-0.09486 x (3.8925 x 0.43251 + 0.9822 x 0.48735))
= 0.2073
Qmix = 0.0065 + 0.2073 = 0.2138 cal/g K
= 0.2138 – 2.488 = - 2.035
Cell Constant = Difference / T
= - 2.035/(-0.0959)
= 21.2275
The procedure is followed for all data points and taken average value. Which is 21.4739
The step wise calculation procedure is presented in Appendix B. The graphs on mole fraction vs.
enthalpy of binary liquid mixtures are drawn using excel sheet.
The measured values of Excess enthalpies using the designed calorimeter for various systems are
compared with the literature values. In this study MTBE with substitute compounds are taken and tabulated
below.
Appendix B
The pure component data, molecular weight, heat capacity and density is collected from the literature.
Methyl Tertiary Buty Ethane (MTBE)(1)_+ Benzene (2)
Component Molecular weight Heat capacity Density (g/cc)
cal/mol K (cal/g. K)
MTBE 88.15 44.79 0.5081 0.7410
Benzene 78.00 31.00 0.3974 0.8675

First data point
Weight of 5 ml of component 1 (w1) = 5 x 0.741 = 3.702g
Weight of 0.5 ml of component 2 (w2)= 0.5x 0.8675= 0.4338 g
Weight fraction = w1/(w1+w2)
= 3.702/(3.702+0.4338) = 0.8951
Mole fracton of component 1,
 2
2
1
1
1
1
1
MW
w
MW
w
MW
w
X

 =
 78
4338.0
15.88
702.3
15.88
702.3

= 0.8831
Average molecular weight = x1*MW1 + (1-X1)*MW2
= 0.8831x88.15 + (1-0.8831)*78
= 87.0
Totals Moles in the mixture = Moles of component 1 (n1) + Moles of component 2 (n2)
= w1/MW! + w2/MW2
= 3.702/88.15 + 0.4388/78
= 0.0476
Q1 = 0.0
Q2, (cal/g k) = -T(w1cp1 + w2cp2 + E)
where E = cell constant = 21.4739
Q2 = -( -0.06457(3.8925  0.43251 + 0.3274  0.48735 + 21.4739))
= 0.5530
QMixt = Q1 + Q2 = 0 + 0.0553 = 0.05530 Cal/g K
QMixt, ( Cla/mol K) = QMixt, ( Cla/g K) /total moles = 0.0553/0.0476
= 11.6825
QMixt = 11.6825x 4.186 = 48.9771 J/mol K
Second Data Point
Weight of 5.5 ml mixture = 4.1358 g
Weight of 0.5 ml component2 = 0.4388 g
Step wise calculation of weight of each component in the mixture:
Step 1: weight of mixture x weight fraction of component 1/average molecular weight of mixture(as in data
point 1)
Weight of component 1 = 4.1358 x 0.8951/87 = 3.702 g
Weight of component 2 in the mixture= 4.1358 – 3.702 + 0.4338 = 8.8675 g
= 4.1358 – 3.702 + 0.4338 = 0.8675 g
Weight fraction = 3.702/(3.702+0.8675)
= 0.8102
Mole fraction =
 78
8675.0
15.88
702.3
15.88
702.3

= 0.7906
Average molecular weight = 0.7906x88.15 + (1-0.7906)*78
= 86.0
Total moles = 3.702/88.15 + 0.8675/78
= 0.531
Q1 is the heat of mixing
Q1 = 0.533*0.8951/87
= 0.0235
Q2, (cal/g k) = -T(w1cp1 + w2cp2 + E)
= -( 3.702*0.5081+0.8675*0.3974+ 21.4739))
= 0.9926
Qmix = 0.0235 + 0.9926 cal/g K
= 1.0162
QMixt, ( Cla/mol K) = QMixt, ( Cla/g K) /total moles = 1.0162/0.0531 = 19.1303
QMixt =4.186* 19.1303 = 80.0796 J/mol K
The procedure is followed for all data points.

Table 4 Comparison of HE
values for MTBE + Benzene system
values for MTBE + Chlorobenzene System
Mole
fraction
Temp
diff. HE
, ca/g % dev
%
Abs.
dev
X1 DT Expt. Lit.
0.0702 -0.0377 61.66723 65.7224 -6.58 6.58
0.1312 -0.0656 101.4375 103.1158 -1.65 1.65
0.1847 -0.0833 121.8941 124.9320 -2.49 2.49
0.2320 -0.0969 134.7273 137.8477 -2.32 2.32
0.2741 -0.1135 150.273 145.4869 3.18 3.18
0.3118 -0.1106 140.068 149.8851 -7.01 7.01
0.3458 -0.1242 150.5544 152.2232 -1.11 1.11
0.3766 -0.1213 141.2712 153.2092 -8.45 8.45
0.4047 -0.1260 141.1457 153.2811 -8.60 8.60
0.4303 -0.1312 141.7238 152.7191 -7.76 7.76
0.4563 -0.1264 155.8413 151.5737 2.74 2.74
0.4856 -0.1215 156.2761 149.6136 4.26 4.26
0.5190 -0.1056 143.4629 146.5411 -2.15 2.15
0.5573 -0.0918 132.8393 141.9060 -6.83 6.83
0.6017 -0.0850 130.5302 135.0060 -3.43 3.43
0.6537 -0.0727 120.0582 124.7196 -3.88 3.88
0.7157 -0.0646 113.819 109.2392 4.02 4.02
0.7906 -0.0419 80.07923 85.7189 -7.04 7.04
0.8831 -0.0235 48.67686 50.1959 -3.12 3.12
86.62
Percent Average Deviation (PAAD) 4.56%
mole
fraction
temp
dif HE, Expt HE, Lit. % dev
% Abs.
dev
X1 DT Cla/g Cla/g
0.0788 0.0385 -71.64272 -66.9476 6.55 6.55
0.1460 0.0864 -148.0908 -143.055 3.40 3.40
0.2041 0.1247 -200.8032 -210.02 -4.59 4.59
0.2549 0.1794 -272.6966 -264.025 3.18 3.18
0.2995 0.1985 -285.8596 -305.821 -6.98 6.98
0.3391 0.2549 -349.1017 -337.345 3.37 3.37
0.3744 0.2623 -342.6953 -360.589 -5.22 5.22
0.4062 0.2921 -365.1651 -377.279 -3.32 3.32
0.4349 0.3147 -377.281 -388.817 -3.06 3.06
0.4609 0.3571 -411.4704 -396.311 3.68 3.68
0.4872 0.3069 -384.2116 -400.949 -4.36 4.36
0.5166 0.2915 -385.3712 -402.623 -4.48 4.48
0.5499 0.2976 -414.3931 -399.995 3.47 3.47
0.5876 0.2741 -404.0098 -391.151 3.18 3.18
0.6310 0.2304 -361.9965 -373.34 -3.13 3.13
0.6813 0.1900 -320.8879 -342.619 -6.77 6.77
0.7403 0.1668 -301.8436 -293.525 2.76 2.76
0.8104 0.1168 -228.0132 -219.373 3.79 3.79
0.8953 0.0582 -122.1843 -115.891 5.15 5.15
80.45
PAAD 4.23%

Fig 2: MTBE + Benzene substituted compounds
The comparison for three binary systems methyl tertiary butyl ether (MTBE) with benzene,
chlorobenzene and Nitrobenzene12
is as shown in the figure 2. From the Tables 4 – 6, it is observed that the
excess enthalpy values for MTBE and benzene are positive (156.3, 153.3 and 48.7, 50.2 maximum and
minimum values for experimental and literature values respectively). The percent average absolute deviation
(PAAD) calculated using eqn. (2) is 4.6%. For MTBE and chlorobenzene, it is negative with -76.6, -66.9 and -
414.4, -402.6 maximum and minimum values for experimental and literature values respectively and PAAD is
4.3%. The values for nitrobenzene are positive to negative with a PAAD of 7.6%. The maximum and minimum
values for experimental and literature are 103.5 , 3.9 & -31.0. The higher percent deviation (7.6%) is due to the
small values of excess enthalpies.
values for MTBE + Nitro
Benzene system
mole
fraction temp dif HE
, Expt. HE
, Lit. % dev
%
Abs.
dev
0.0790 -0.03460 64.9066 57.12924 11.982 11.982
0.1465 -0.05047 88.6246 83.18271 6.140 6.140
0.2047 -0.05184 85.5674 93.53545 -9.312 9.312
0.2555 -0.06652 103.5125 95.70375 7.544 7.544
0.3002 -0.06061 89.4404 93.53582 -4.579 4.579
0.3399 -0.06734 94.4018 89.08179 5.635 5.635
0.3753 -0.06627 88.6210 83.47089 5.811 5.811
0.4070 -0.05681 72.6937 77.34162 -6.394 6.394
0.4357 -0.05516 67.6311 71.06154 -5.072 5.072
0.4618 -0.04823 61.6576 64.84383 -5.168 5.168
0.4881 -0.04726 61.8176 58.15572 5.924 5.924
0.5175 -0.03460 47.8459 50.24988 -5.024 5.024
0.5507 -0.02999 43.0956 40.93145 5.022 5.022
0.5885 -0.02176 32.4054 30.00963 7.393 7.393
0.6318 -0.00983 15.3460 17.36053 -13.128 13.128
0.6821 -0.00280 3.9234 3.0949 21.116 21.116
0.7409 0.00670 -13.1272 -12.0003 8.584 8.584
0.8110 0.01315 -26.4091 -25.2766 4.288 4.288
0.8956 0.01474 -31.0094 -28.9053 6.785 6.785
144.9
PAAD 7.6%

values for DMF + MIBK System
values for DMF + MEK System
Fig.3: DMF with ketones
mole
fraction
temp
dif
HE
,
Expt.
HE
,
Lit.
%
dev
%
Abs.
dev
0.1038 -0.0291 46.469 44.616 3.99 3.99
0.1880 -0.0559 81.993 87.315 -6.49 6.49
0.2578 -0.0832 112.791 107.080 5.06 5.06
0.3165 -0.0954 120.398 116.434 3.29 3.29
0.3667 -0.1002 118.366 122.495 -3.49 3.49
0.4099 -0.1112 123.542 127.564 -3.25 3.25
0.4477 -0.1289 135.242 131.977 2.41 2.41
0.4809 -0.1419 141.294 135.551 4.06 4.06
0.5103 -0.1414 134.135 138.101 -2.96 2.96
0.5366 -0.1584 143.336 139.564 2.63 2.63
0.5626 -0.1405 144.914 139.975 3.41 3.41
0.5914 -0.1182 129.089 138.935 -7.63 7.63
0.6232 -0.1257 139.480 135.671 2.73 2.73
0.6587 -0.1040 121.933 129.232 -5.99 5.99
0.6984 -0.1028 124.170 118.633 4.46 4.46
0.7432 -0.0846 106.351 103.220 2.94 2.94
0.7942 -0.0597 79.388 83.368 -5.01 5.01
0.8527 -0.0446 61.985 61.195 1.28 1.28
0.9205 -0.0280 40.099 38.678 3.54 3.54
74.63
PAAD 3.93%
Mole
fraction
temp
dif
HE
,
Expt. HE
, Lit.
%
dev
%
Abs.
dev
0.1391 -0.0756 162.723 139.003 14.58 14.58
0.2443 -0.1179 221.623 215.641 2.70 2.70
0.3265 -0.1432 242.307 257.387 -6.22 6.22
0.3926 -0.1758 270.856 285.953 -5.57 5.57
0.4469 -0.2085 295.428 309.162 -4.65 4.65
0.4923 -0.2407 316.253 328.827 -3.98 3.98
0.5308 -0.2850 349.362 345.031 1.24 1.24
0.5639 -0.2916 335.523 357.669 -6.60 6.60
0.5926 -0.3190 346.031 366.825 -6.01 6.01
0.6178 -0.3683 378.277 372.783 1.45 1.45
0.6423 -0.3156 355.885 376.137 -5.69 5.69
0.6689 -0.3442 398.299 376.385 5.50 5.50
0.6978 -0.3284 392.669 371.922 5.28 5.28
0.7293 -0.2970 368.535 360.660 2.14 2.14
0.7637 -0.2685 345.255 340.054 1.51 1.51
0.8016 -0.2258 303.091 307.351 -1.41 1.41
0.8434 -0.1958 271.337 260.136 4.13 4.13
0.8899 -0.1316 190.022 196.987 -3.67 3.67
0.9417 -0.0794 116.019 116.019 0.00 0.00
82.32
PAAD 4.33%

Similar observation were made (Tables7, 8) with dimethyl formamide(DMF) with methyl ethyl ketone
(MEK) and mehyl isobutyl ketone (MIBK)13
systems. The PAAD are 3.9 % and 4.3% for DMF + MEK and
DMF+MIBK respectively. From the figs.2 and 3, it can be seen that the experimental values are in good
agreement with literature values.
Table 9 Experimental values of HE
for DME + Benzene System
Mole
fraction temp dif
HE
,
Expt. HE
, Lit. % dev
% Abs.
dev
0.0950 -0.1013 201.26 197.705 1.766 1.766
0.1735 -0.0958 174.28 189.773 -8.890 8.890
0.2395 -0.0956 161.37 160.594 0.481 0.481
0.2957 -0.1003 158.1 142.251 10.025 10.025
0.3442 -0.0912 136.77 134.310 1.798 1.798
0.3865 -0.1034 144.62 132.089 8.665 8.665
0.4236 -0.1023 137.16 132.161 3.644 3.644
0.4565 -0.0976 125.33 132.721 -5.897 5.897
0.4858 -0.1018 124.22 133.028 -7.091 7.091
0.5121 -0.1095 127.82 132.911 -3.983 3.983
0.5121 -0.1086 126.16 132.911 -5.351 5.351
0.5384 -0.0946 115.82 132.377 -14.296 14.296
0.5675 -0.0983 125.7 131.442 -4.568 4.568
0.6000 -0.1101 144.37 130.395 9.680 9.680
0.6363 -0.0997 137.33 130.095 5.269 5.269
0.6774 -0.0965 139.2 132.326 4.938 4.938
0.7241 -0.088 135.98 140.051 -2.994 2.994
0.7777 -0.1034 166.91 156.547 6.209 6.209
0.8400 -0.0982 169.25 179.709 -6.180 6.180
0.9130 -0.1023 179.57 177.836 0.966 0.966
112.690
5.63%
Fig. 4 DME + Benzene
The binary mixtures for Dimethoxyethane( DME) +Benzene set of results was fitted by the flowing equation to
calculate the enthalpy.
HE
(j/mol) = 3553.1(x1-x2)4
- 159.31(x1-x2)3
+ 221.25(x1-x2)2
- 10.094(x1-x2) + 532.07 (2)
Excess enthalpy data is generated for a binary system dimethoxyethane and benzene at room
temperature. Fig. 4 represents the experimental data and polynomial equation (2). The data along with the
calculated values using equation (2) is reported in Table 8. The percet average absolute deviation over the entire
composition range is 4.3%.
Acknowledgements
I would like to thank my professor K. Malakondaiah. For his guidance and I would equally extend my
dexterous attitude to Dr.Y.V.L. Ravikumar, Technical officer IICT and Dr. B. Satyavathi, Principal Scientist
IICT for their assistance and constant backup by helping throughout for the development of project because of
which this project could be completed successfully.

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