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Article history: The limitation of the conventional fluids to facilitate cooling/heating rates remains the primary basis for
Received 8 January 2016 exploring alternative heat transfer nanofluids. Research efforts on nanofluids have evolved over the past
Received in revised form two decades in establishing extensive literature. Several models for thermophysical properties were
10 March 2016
made available to characterize the behaviors of diverse individual nanofluids. However, lack of reason-
Accepted 15 August 2016
able agreement between theory and experimental results has been a limiting factor for the development
Available online 27 August 2016
of a unified nanofluid model for thermal conductivity. Existing models for thermo-physical properties of
Keywords: nanofluids such as density, specific heat, thermal conductivity, and viscosity are critically surveyed and
Composite Nanoparticles appropriate equations are extended for composite nanofluids. Consequently, based on reliable models
Nanofluids
identified predictions for thermal conductivity and viscosity for composite nanofluids are presented.
Properties
Overall results show that existing thermophysical models for density and specific heat are valid for all
Influencing parameters
water based oxide nanofluids for both single material and composites whereas models for thermal
conductivity and viscosity show selective response but have the versatility for predicting the behavior of
single and composite nanofluids within acceptable deviation.
& 2016 Elsevier Ltd. All rights reserved.
Contents
1. Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 655
2. Properties of single material nanofluids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 655
2.1. Density . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 656
2.2. Specific heat. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 656
2.3. Thermal conductivity. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 657
2.3.1. Effect of particle volume concentration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 658
2.3.2. Effect of temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 658
2.3.3. Effect of particle size . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 659
2.3.4. Effect of particle shape . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 659
2.3.5. Influence of base fluid . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 659
2.3.6. Influence of material . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 660
2.3.7. Effect of pH . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 660
2.3.8. Modeling of thermal conductivity in nanofluids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 660
2.3.9. Validation of the thermal conductivity models . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 660
2.4. Viscosity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 661
2.4.1. Effect of particle volume concentration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 663
2.4.2. Effect of temperature. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 663
2.4.3. Effect of particle size . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 663
2.4.4. Effect of particle shape . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 663
2.4.5. Effect of pH . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 665
2.4.6. Modeling of viscosity in nanofluids . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 665
n
Corresponding author.
http://dx.doi.org/10.1016/j.rser.2016.08.036
1364-0321/& 2016 Elsevier Ltd. All rights reserved.
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 655
the convective heat transfer coefficients [28]. The thermo-physical that the experimental data is consistent with the values estimated
properties of nanofluids such as density, specific heat, thermal with Eq. (1). Khanafer and Vafai [38] presented an equation for the
conductivity, and viscosity are essential and must be known in estimation of Al2O3 nanofluid density as a function of particle
advance. A number of models for the evaluation of SmNf proper- volume concentration and temperature given by:
ties have been developed. However, the development of general-
ρnf , T = 1001.064 + 2738.6191 ϕp − 0.2095 Tnf (2)
ized equations applicable for a wide range of parameters can be a
challenging task. Equations for the estimation of nanofluid density, where, Tnf is the nanofluid temperature and ϕp is particle volume
specific heat, thermal conductivity and viscosity presented in the
concentration. Eq. (2) is developed for Al2O3 nanofluid valid in the
literature are discussed with the exception of thermal diffusivity
range of volume concentration of 0–4.0% and temperature 5–40 °C.
and surface tension.
Eq. (2) is in good agreement with the experimental data when
compared to values evaluated with Eq. (1) with a maximum de-
2.1. Density
viation of 0.6%. Hence, Eq. (1) can be used to evaluate the effective
density of various nanofluids.
Addition of a small fraction of solid nanoparticles to a base li-
quid would systematically enhance the density of the mixture [12].
This is because the density of solids is greater than liquids. Mod- 2.2. Specific heat
eling density in nanofluids requires the estimation of the con-
stituent’s material densities and volume concentrations. Studies Nanofluid specific heat can be expressed as a blend of heat
have been undertaken to determine the density of nanofluids for capacities of solid and liquid phases when the phases are in
different particle sizes (1–100 nm), temperatures (5–60 °C), and thermal equilibrium. Xuan and Roetzel [49] presented an equation
volume concentrations (0–5.0%). For example, Ho et al. [45] ob-
served approximately a 10% increase in the density of
Al2O3(33 nm)/water nanofluid at 4.0% vol. when the density of the
nanofluid decreased by 5% and temperature increased from 25 to
40 °C. Heyhat et al. [46] reported the density of Al2O3(40 nm)/
water nanofluid to increase by a maximum of 3% for 2.0 vol.%
concentration. However, a maximum decrease of 3.8% in density at
a temperature of 60 °C was observed. Teng and Hung [47] reported
similar observations of decrease in density with concentration.
The effective density of nanofluid ρnf can be expressed analy-
tically based on mass balance using the conventional mixing
theory as:
( )
ρnf = 1 − ϕp ρbf + ϕpρp (1)
where, ρnf is the effective density of the nanofluid with the addi-
tion of ϕp volume fraction of nanoparticles. The density of SmNf at
different particle volume concentrations is depicted in Fig. 1. The
densities of Al2O3 and TiO2 nanofluids enhanced by 14% and 16%
respectively when dispersed in water for 5% volume concentration
at 25°C. This observation is consistent with the experimental data Fig. 1. Comparison of single material nanofluid density with Eq. (1) for different
reported by Pak and Choi [48]. It can also be observed from Fig. 1 particle volume concentrations.
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 657
Table 1
Specific heat models.
1
4. Vajjha [52] ⎡ ⎛ c
p, p ⎟
⎞⎤ Al2O3, 2SiO2, 3ZnO/ Water 1
44, 220, 377 1,2
0–10 20–7 42–90
⎢ ( A × T ) + B⎜⎜ ⎟⎥
⎢ ⎝ cp, bf ⎠ ⎥
cp, eff =⎢ ⎥cp, bf
⎢ (
C + ϕp ) ⎥
⎢⎣ ⎥⎦
1 1 1
A = 0.0008911, B = 0.5179 C = 0.4250
2 2 2
A = 0.001769, B = 1.1937 C = 0.8021
3 3 3
A = 0.0004604, B = 0.9855 C = 0.2990
1
5. Yiamsawasd et al. [51] ⎡ ⎛ Cp, p ⎞⎤
D Al2O3, 2TiO2–/Water 1
120, 221 0–8 15–65
cp, eff = ⎢ A ϕpBT C ⎜ ⎟⎥ cp, bf
⎣ ⎝ Cp, bf ⎠⎦
1 1
A = 1.249458, B = − 0.05846
1 1
C = 0.006467, D = − 0.17236
2 2
A = 1.387402, B = − 0.06425
2 2
C = 0.001124, D = − 0.21159
6. Sekhar and Sharma [50] ⎛ Tnf ⎞
−0.3037
⎛ dp ⎞
0.4167
⎛ ϕp ⎞2.272 Al2O3, CuO, TiO2, SiO2/–Water 15–50 0–4 20–50
Cp, eff = 0.8429 ⎜ 1 + ⎟ ⎜1 + ⎟ ⎜1 + ⎟
⎝ 50 ⎠ ⎝ 50 ⎠ ⎝ 100 ⎠
cp, nf
(1 − ϕ ) ρ
p
c
bf bf
+ ϕpρp cp
ρnf (3)
Table 2
Thermophysical properties of some selected nanoparticle materials at 300 K.
2.3.1. Effect of particle volume concentration TiO2(33 nm)/water nanofluid increased by approximately 15% for a
Regardless of the type of base fluid, addition of solid nano- volume concentration of 5.0% compared to water. In addition to
particles to a fluid is expected to affect the thermal conductivity of the observations of these investigators, several experimental stu-
the mixture [60–70]. Pioneering work of Masuda et al. [60] with dies [45,54,76,80–92] for water based oxide nanofluids have re-
Al2O3(13 nm)/water nanofluid obtained a maximum enhancement ported knf enhancements with increase in concentration. The re-
of 32% in knf as particle volume concentration is increased from sults presented demonstrate a linear increase in knf with particle
1.0 to 4.3%. Lee et al. [61] reported a 10% increase in knf of concentration.
Al2O3(38 nm)/water nanofluid with increase in particle con- Evidently, the addition of nanoparticles to base liquid enhanced
centration from 0 to 4.3% vol. Wang et al. [62] dispersed Al2O3 the thermal conductivity of the suspension and the degree of the
nanoparticles in water and observed enhancement in knf of the enhancement depended on the volume fraction of the particles
suspension. For a particle concentration of 3% vol. knf was observed added. The reasons for the enhancement is attributed to several
to increase by 12% as compared to base liquid. Zhang et al. [63] microscopic phenomena such as particle dynamic effect, liquid
reported that knf of Al2O3(20 nm)/water enhanced by 11.7% when layering on the surface of nanoparticles, and particle clustering
the concentration was increased to 4.3% vol. Chandrasekar et al. [58].
[64] observed enhancement in knf with increasing particle con-
centration of Al2O3(43 nm)/water nanofluid. The increase in knf of 2.3.2. Effect of temperature
about 3.43%, 7.52%, and 9.7% was observed with concentrations of Studies on the effect of temperature variation on knf are limited
1%, 2% and 3% respectively. The knf enhancement of 8% was re- in the literature despite the considerable interest to utilize nano-
ported by Kim et al. [65] for Al2O3(38 nm)/water nanofluid in the fluid for higher temperature applications [28]. Das et al. [83] were
concentration range from 0 to 3.0% vol. A comparable value of the early investigators to report the dependence of temperature on
enhancement was also reported by Patel et al. [66] with thermal conductivity of nanofluids. They observed 3–4 fold en-
Al2O3(45 nm)/water nanofluid. hancement of knf with Al2O3 (38 nm)/water in the range of tem-
Jahanshahi et al. [69] demonstrated a 32% increase in knf with perature of 21–51 °C. Chon et al. [81] observed 8.2% increase in knf
SiO2(12 nm)/water as the concentration increased from 1 to 4.0 % with Al2O3(150 nm)/water at 1.0 vol%. However, Murshed et al.
vol. concentration. The knf measurements for SiO2(12 nm)/water in [93] reported relatively higher knf values of about 10.6% under
different particle concentrations have been carried out by Tavman similar conditions. Li and Peterson et al. [68] reported up to 2 fold
et al. [71]. The maximum knf enhancement of 2.4% was realized at increase of knf with Al2O3(36 nm)/water in the temperature range
the highest concentration of 4.0% vol. concentration. Kang et al. of 20 °C to 60 °C. The enhancement in knf at 2% and 4.0% vol.
[72] noticed that the knf of SiO2 of water based nanofluids in- concentrations respectively was reported as 11%, 23% at 30 °C and
creased by 5% with particle loading from 0 to 6.0% vol. con- 16, 28% at 35 °C respectively. Patel et al. [66] measured the knf of
centration. Many other researchers also observed an increase in knf 3.0% vol. concentration of Al2O3 (45 nm)/water using temperature
of SiO2/water nanofluid with increase in concentration at room oscillation technique. They reported knf enhancement of 8–13%
temperature [73–75]. when the temperature was enhanced from 30 °C to 40 °C. How-
Experimental studies with CuO/water show a considerable ever, Barbés [54] reported 5–7.0% knf enhancement in the same
enhancement in knf with increase in volume concentration range of temperatures.
[68,62,66]. The knf of dilute suspension containing CuO(23 nm)/ Ferrouillat et al. [74] have estimated the knf of SiO2(22 nm)/
water nanofluid improved by approximately 12% with increasing water nanofluid using steady state principle. They noticed knf of
concentration from 0 to 3.4 vol% [61]. However, higher enhance- the suspension to increase from 1.6% to 1.8% with temperature
ment of up to 16% with CuO(47 nm)/water nanofluid was achieved from 25 to 50°C at a volume concentration of 2.3% in comparison
at a lower concentration of 0.8 vol% by Sundar and Sharma [76]. to water. Hussein et al. [73] reported 11.7–13.3% greater knf en-
Khedkar et al. [77] obtained a maximum enhancement of 17.7% for hancement at 1.5% vol. concentration of SiO2(30 nm)/water in the
knf at 5% concentration with CuO(25 nm)/water. In a recent work same temperature interval.
reported by Minakov et al. [78], CuO(55 nm)/water nanofluid ex- Temperature dependent thermal conductivity for CuO/water
hibited significant knf enhancement of 40% at 2.0% vol. nanofluid has been reported by Das et al. [83]. They observed a
concentration. considerable increase in the nanofluid knf particularly at higher
Duangthongsuk and Wongwises [67] reported a maximum knf temperatures. At 1.0 vol%, the knf of CuO(28 nm)/water increased
enhancement of 3% and 7% with TiO2 (21 nm)/water nanofluid for by 6.5% and 36% with the increase of temperature from 21 to 51 °C.
0.2 and 2.0% vol. concentration respectively. The results demon- Brownian motion of the nanoparticles was suggested to be the sole
strated higher enhancement of 6% and 5% in knf for the low and reason for the enhancement. Mintsa et al. [94] observed a 22.7%
high concentrations compared to values obtained by Masuda et al. enhancement in knf for 3.3% vol. concentration of CuO(36 nm)/
[60] and Zhang et al. [63] with particle size of 27 and 33 nm re- water nanofluid with an increase in temperature from 21 °C to
spectively Yiamswasd et al. [70] measured the knf of TiO2(21 nm)/ 40 °C. The knf enhancement of 34% and 44% was observed by Li and
water suspension for particle concentrations of 1.0, 2.0, and 4.0. It Peterson [68] in their experimental investigation with CuO
was observed that knf of the nanofluid enhanced by 2%, 5%, 10% (29 nm)/water for temperatures of 30 °C and 35 °C respectively for
respectively. Further, Saleh et al. [79] showed that knf of 4% vol. concentration. The knf enhancement of 8.5–16.5% with CuO
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 659
(31 nm)/water was reported by Patel et al. [66] in temperature 10 nm in diameter has been documented by Shima et al. [102],
range of 20–60 °C. which is in deep contrast with the observations of Jang and Choi
Variation of knf with temperature for TiO2 nanoparticles in [101] as well as Feng et al. [100]. However, Shima et al. [102] noted
water with temperature has been investigated by Duangthongsuk that the growth of small particles into fractal-like aggregate
and Wongwises [67] using transient hot-wire (THW) principle. structure in the base fluid may be the reason for the increase in the
Zhang et al. [63] however employed a modified THW system to knf , when the particle size was increased from 2.8 to 9.5 nm.
measure the knf of TiO2(33 nm)/water nanofluid. Their results The effect of particle size on the knf enhancement in nanofluids
show a knf enhancement of about 5.6% and 6.4% at temperatures of can be explained by two factors: the increase in surface-area-to-
20°C and 60°C respectively for 2.55% vol. concentration. Further, volume-ratio and phonon effect. As the particle size decreases, the
Saleh et al. [79] reported the knf enhancement of 11% and 17% with surface area of the nanoparticles become enlarged and thereby
TiO2(33 nm)/water when the temperature increased from 15 to leading to enhanced thermal conductivity. Likewise, the kp will
50 °C for 3.0% vol. concentration. decrease when the phonon mean free path is of the same order as
From the experiments undertaken, it can be seen that knf of the particle size. This is due to the decrease in intensity of the
nanofluids increase with temperature. This can be due to Brow- main carrier (phonon) at the particle interfacial locations [88].
nian motion of the nanoparticles which is a strong function of
temperature resulting in the lowering of viscosity. The stronger 2.3.4. Effect of particle shape
the Brownian motion, the greater is the contribution to micro- In the literature, a limited number of studies are reported re-
convection with consequent enhancement in effective con- lating to the effect of particle morphology or aspect ratio on the
ductivity of the nanofluid [93]. nanofluid thermal conductivity [87,103,104]. Timofeeva et al. [87]
reported the knf enhancement of Al2O3/50:50 EG-water mixture as
2.3.3. Effect of particle size a function of particle shape. Higher thermal conductivity of ap-
According to Wang and Mujumdar [95] the value of knf can be proximately 5% of the nanofluid was observed when dispersed
altered by varying the particle size. By decreasing the particle size, with particles having the shape of cylinders as compared to 2.9%
the surface area to volume ratio increases, and consequently the obtained with platelets. Murshed et al. [103] revealed that rod-
knf of the nanofluid would increase. Studies show a direct corre- shaped TiO2 nanoparticles of dimension (Ø10 nm 40 nm) exhibit
lation between particle size and knf enhancement of nanofluids. greater increase in knf compared to spherical-shaped (15 nm) na-
The water based oxide nanofluids mostly indicate a decrease in knf noparticles dispersed in aqueous medium. They observed the en-
with increase in particle size. Teng et al. [96] reported Al2O3 knf hancement for the rod and spherical shaped particles as 33% and
enhancement of approximately 12.8% and 5.3% respectively with 30% respectively. It can be concluded from the experimental data
nanoparticles of 20 and 100 nm size at room temperature. Chon that nanofluids dispersed with particles of large length to dia-
et al. [81] observed a knf enhancement of 4.8% and 15.8% with meter ratio can have greater knf enhancements owing to large
particle size of 150 and 11 nm respectively for Al2O3/water nano- surface area facilitating heat conduction through the fluid.
fluid. Similar conclusions have been reported by Mintsa et al. [94]
with (36, 47 nm) and He et al. [97] with (95, 145 and 210 nm) set of 2.3.5. Influence of base fluid
particle sizes respectively, including a recent study by Kazemi- A number of investigators have reported the dependence of knf
Beydokhti et al. [98] with Al2O3 (12, 26, 48, 36, and 47)/water on the inherent conductivity of the base fluid kbf [54,89,98,104].
nanofluid. The reference value of kbf for common heat transfer fluids at 300 K
In contrast, there are also a few reports on the increase in knf are given in Table 3. Hwang et al. [105] observed knf enhancement
with increase in particle size. Beck et al. [88] observed a decrease of 3% and 9% with CuO(35 nm) dispersed in deionized water (DIW)
in k enhancement with increase in Al2O3 particle size from 2 to and ethylene glycol (EG) respectively. The value of knf obtained
282 nm. The rate of knf enhancement was pronounced for particles with CuO(33 nm)/EG nanofluid are greater than those presented
between 10–50 nm. This behavior was attributed to increase in by Eastman et al. [106], which corresponds to 4.8% in DIW and
phonon scattering with decrease in particle size. Moreover, mo- 9.0% in EG base liquids respectively. Patel et al. [66] reported knf
lecular dynamics simulation based on Stilling–Weber (SW) po- enhancement of 6% and 8% in DIW and EG respectively with
tential model for SiO2 nanoparticles of size between 2 and 12 nm Al2O3(23.6 nm) at 1.0% volume concentration determined at 20°C.
predicted a linear increase in k ratio. However, such an increase However, the enhancement in knf dispersed with SiO2(12 nm) in
was considered anomalous, which is attributed to proliferation in water are observed to be 1.0% greater than with EG based ex-
the phonon mean path [99]. perimental data of Kazemi et al. [98]. This enhancement is at-
The fractal theorem and analytical modeling has been em- tributed to hydrophilic affinity of SiO2(12 nm) nanoparticles to
ployed by Feng et al. [100] and Jang and Choi [101] respectively to water molecules resulting in a stable dispersion.
study the influence of particle agglomeration on knf enhancement The investigators observed greater enhancements with EG as
in nanofluids. Results show an exponential decrease in knf ratio compared to DIW. Therefore, it can be deduced that base liquid
with increase of particle size above 10 nm, which suggest that at a with higher thermal conductivity need not be the deciding factor
certain critical diameter of 10 nm the nanoparticles are not effi- for obtaining higher enhancement in thermal conductivity as the
cient enough probably due to the reduced particle conductivity enhancement is related to the dispersed nanoparticle. Hence, a
and increased solid-liquid interfacial thermal resistance. Never- stable nanofluid of certain net electric charge reflected through
theless, an increase in the knf ratio with particles of less than zeta potential in the range between 740 and 760 mV may offer
Table 3
Thermo-physical properties of some selected conventional cooling fluids at 300 K.
Base fluid Thermal conductivity Density Specific heat Thermal diffusivity 10 8 Reference
Deionized water (DIW) 0.607 998 4200 14.55 Sattler et al. [58]
Ethylene glycol (EG) 0.255 1111 2400 9.385 Sattler et al. [58]
Engine oil (EO) 0.145 884 1900 8.740 Sattler et al. [58]
660 S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678
better thermal transport capabilities. This means that a nanofluid used by various investigators for characterization of the nanofluids
at optimized state of pH or surface would be likely to facilitate is given in Table 4.
phonon transport through increase in effective charged sites re-
sulting in enhanced thermal conductivity. 2.3.8. Modeling of thermal conductivity in nanofluids
A considerable number of mechanisms have been suggested to
2.3.6. Influence of material explain the observed enhancement of nanofluid thermal con-
The thermal conductivity of material can exert significant in- ductivity. The mechanisms for enhanced thermal conductivity can
fluence over knf of nanofluid. As such, a bulk material of higher k be classified into two main groups viz., the static mechanism
would be expected to exhibit greater knf enhancement when dis- which assumes the particles to be stationary while suspended in
persed in base fluid as compared to one with lower conductivity base liquid. Thus, microscopic phenomenon of nanolayer [114],
under similar conditions. A comparison of k of typical oxide nano interfacial resistance [115], aggregation and percolation [116] may
materials used in nanofluid preparation are given in Table 3. be responsible for the enhanced conductivity. The dynamic me-
The influence of material properties on nanofluid knf en- chanism which considers the particles to be in random motion as
hancement have been investigated by several researchers in the case of the Brownian motion and micro convection to be
[61,62,66,89]. Murshed et al. [93] observed about 6.2% increase in responsible for knf enhancement based on the works of Lee et al.
knf at 1.0% vol. concentration of Al2O3(80 nm)/water at 30°C. [117], Keblinski et al. [118], Michaelides [119].
However, at the same particle concentration and temperature, The evaluation of knf of nanofluids can be a complex process
Patel et al. [66] reported two-fold enhancement in knf with Cu due to number of parameters involved in the analysis. Never-
(80 nm)/water nanofluid. Kim et al. [65] reported 14.2% and 11.4% theless, the thermal conductivity of nanofluid knf can be modeled
enhancements in knf with ZnO(10 nm)/water and TiO2(10 nm)/ based on two known approaches viz., the mathematical methods,
water at 20°C for a nanofluid concentration of 3.0%. In contrast, which is based on hypothesis and semi-empirical methods which
others [107,108] maintain that kp is not an indicator for enhanced inherently blends theory with experimental data.
fluid conductivity as in the case of Zhu et al. [107] who demon- Mathematical models [21,26,27,38,45,46,66,68,81,93,101,106,
strated 34.8% enhancement with Fe3O4(10 nm)/water nanofluid 114,120–144] for the estimation of nanofluid thermal conductivity
for a particle concentration of 3.0% vol. concentration, while given in Table 5 through Eqs. (7)–(30) have limited applicability
Al2O3(13 nm) with 22% despite the fact that k of bulk Al2O3 is ty- with respect to the effects of particle size, temperature, particle
pically higher than that of Fe3O4. Shima et al. [108] observed knf distribution, and pH. As a result, these models are unable to pre-
enhancements of hexadecane based Ag(7 nm) and Fe2O3(7.5 nm) dict the experimental data of within acceptable limits. However,
nanofluids are approximately the same at 2% concentration. It can semi empirical models [48,94,145–148] listed in Table 6 through
be summarized based on the investigations undertaken by various Eqs. (31)–(50) are derived using experimental data. Most of the
investigators that material properties of the particles can have a models developed are functions of temperature, particle con-
significant influence on nanofluid knf. The enhancements can be centration, clearly a majority of equations proposed are valid for a
sustained over a period of time, if the nanofluid remains in a specific nanofluid and particle size and could not be used for
uniformly dispersed state and free from distorted aggregation. comparison with other equations. The models can be categorized
to reflect this nature with the exception of the model presented by
2.3.7. Effect of pH Corcione [27] and Sharma et al. [26] in Eqs. (49) and (50) applic-
The observed variation in nanofluid knf by various investigators able for spherical particles dispersed in water. The models de-
may be due to the presence of temperature gradient at different scribing the mechanism of thermal conductivity enhancement are
values of pH [109–113]. Yoo et al. [109] observed that knf en- presented through Figs. 3–5.
hancement can be achieved with pH adjustment of the nanofluid.
The researchers found 2.7% higher knf increase with Al2O3(50 nm)/ 2.3.9. Validation of the thermal conductivity models
water at pH 10.94 compared to Al2O3(50 nm) dispersed in buffered Comparison of knf for SmNf with Eqs. (49) and (50) for various
neutral solution of pH 7 for concentration of 1.5% vol. Wang and particle concentration, temperature, and particle sizes is presented
Fang [113] observed a maximum value of knf Al2O3(25–60 nm) through Figs. 6–9. It can be observed from Fig. 6 that Eqs. (49) and
when the surface charge on a particle is far away from the iso- (50) predict the thermal conductivity data of Patel et al. [66], Kim
electric point (IEP). A maximum enhancement in knf of 9% and 10% et al. [65], Yoo et al. [109] with Al2O3/water nanofluids for volume
were observed at an optimum value of pH ≈8.0 for 0.1 wt% and concentration less than 5.0%. Eq. (50) is observed to over predict
0.2 wt% respectively. It was further explained that the repulsive the experimental data of Al2O3 nanofluids to a maximum of 20% as
forces between the particles or rather high zeta (ζ) potential sus- compared to Eq. (49) which exhibited a marginal deviation of 7.4%
tain the fluid in a highly dispersed state. Xie et al. [112] discussed at higher particle concentrations.
about the dependence of knf enhancements with pH based on the Thermal conductivity data for water based CuO nanofluid of
experimental observations with Al2O3(35 nm)/water and Diamond Zhu et al. [149], Lee et al. [61], Khedkar et al. [77], Sahooli et al.
(5–10 nm)/EG nanofluids. The repulsive forces on the surface of [150] is depicted in Fig. 7 for concentration o5.0% vol. The ex-
nanoparticles increase with pH value of a suspension from the IEP, perimental data is in good agreement with the predicted values
which give rise for enhanced particle mobility in the suspension. from Eqs. (49) and (50) especially at concentrations between 0 and
This phenomenon trigger micro-convection and result in transport 2.0% vol. However, the average deviation based on the Eqs. (49)
efficiency. and (50) from the experimental data is greater by 1.9% and 3.1%
The results from the investigation support the relationship respectively for concentrations 42.0%.
between pH and stability of the nanofluids. Large aggregation re- The thermal conductivity experimental data of Ferrouillat et al.
sults when particle-particle repulsion force is weak. As pH shifts [74] for SiO2(22 nm)/water nanofluid shown in Fig. 8 deviated
towards the acidic region, surface charge density increases and from the predicted values of Eqs. (49) and (50) by approximately
thus particle aggregation is inhibited. Once dispersion stability is (8.0%, 9.2%) and (0.3%, 0.5%) respectively at volume concentrations
attained, higher values of thermal conductivity can be ensured of 2.3% and 4.0% respectively.
[112,80]. However, according to Timofeeva et al. [87] a change in Fig. 9 display a comparison of knf data of Yiamswasd et al. [70]
pH can possibly affect the viscosity without negative consequences and Kim et al. [65] with predicted values estimated with Eq. (49)
to the knf enhancement of the nanofluids. Summary of equipments and (50) for TiO2/water at different concentrations. Eq. (49) exhibit
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 661
Table 4
Materials and characterization equipments.
close agreement with the experimental data of TiO2 (21 nm) and 2.4. Viscosity
(71 nm) nanofluids while Eq. (50) under predicted the data by a
maximum deviation of 3.5% and 2.5% respectively. It is also ap- Fluids encounter internal resistance to flow through pipes due
parent from Fig. 9 that, in the concentration range between 0 and to viscosity. The magnitude of heat transfer depends on the vis-
5.0% vol., the deviation of the data increased with concentration. cous state of the fluid rather than on thermal conductivity [151]. It
Since the difference between the predicted values and the ex- is important in nanofluid flow to attain a compromise between
perimental data of various single material nanofluids is low, Eqs. thermal conductivity and viscosity enhancement. For example, a
(49) and (50) can be extended to predict the thermal conductivity viscous base fluid can offset the thermal conductivity since its heat
of composite nanofluids. Summary of the comparisons of the transfer capabilities hinged upon the contributions due to Brow-
thermal conductvity predictions with regression Equations (49) nian and micro-convection effects, which are important mechan-
and (50) has also been given in Table 7. isms for enhanced thermal performance [152].
662 S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678
Table 5
Theoretical thermal conductivity models.
ϕp Particle Shape
⎡
k¯ = ⎢
( keff − kshell) ( 2kshell + kp) − ( kp − kshell) ( 2kshell + keff ) λ ⎤⎥
⎢⎣ ( 2keff + kshell) ( 2kshell + kp) + 2 ( kp − kshell) ( kshell − keff ) λ ⎥⎦
–
20. Leong et al. [114]
( kp − klr ) ϕpklr⎡⎢⎣ 2β13 − β 3 + 1⎤⎥⎦ + ( kp + 2klr ) β13⎡⎢⎣ ϕpβ 3( klr − kbf ) + klr ⎤⎥⎦ ⎛ δ ⎞
Spherical
keff = ⎡ ⎤
, β = ⎜1 + ⎟
β 3 kp + 2klr − kp − klr ϕp ⎢⎣ β 3 + β 3 − 1⎥⎦
( ) ( ) ⎝ ap ⎠
1 1
–
21. Murshed et al. [93]
( kp − klr ) ϕpklr⎡⎣⎢ β12 − β2 + 1⎤⎦⎥ + ( kp + klr ) β12⎡⎣⎢ β2ϕp( klr − kbf ) + kbf ⎤⎦⎥ ⎛ δ ⎞
Cylindrical
keff = ⎛ 2
, β1 = ⎜ 1 + ⎟
⎡ ⎤⎞ ⎝ 2ap ⎠
β k + klr ) − ( kp − klr ) ϕp ⎣⎢ β 2 + β 2 − 1⎦⎥
⎝ 1( p
⎜ ⎟
1 ⎠
22. Jang and Choi [101] dbf C¯ R.M.dp – Spherical
( )
keff = 1 − ϕp kbf + kpϕp + C1 kbf Re2dpPrϕp,
dp
C1 = 18 × 106 , Re =
v
,
Do
C¯ R.M. =
λbf
( ) (
f T , φp = −6.04 φp + 0.4705 T + 1722.3 φp − 134.63 ) ( )
⎡ k + 2k + 2 – –
25. Prasher et al. [136]
keff = ( 1 + ARemPr0.3ϕp)
( kp − kbf ) ϕp ⎤⎥ k
⎢ p bf
( kp − kbf ) ϕp ⎥⎦ bf
⎢⎣ kp + 2kbf −
26. Yang [139] ⎡ k + 2k + 2 k − k ϕ ⎤ – –
keff = 157.5 ϕpC up2τ + ⎢
p bf ( p bf ) p ⎥ k , up =
3KBT
,τ=
mp
⎢⎣ kp + 2kbf − ( kp − kbf ) ϕp ⎥⎦ bf mp 6πμbf rp
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 663
Table 5 (continued )
ϕp Particle Shape
⎡ – –
27. Wang et al. [130]
( ) ( ) ⎤⎥
∞
kcl rcl n rcl
⎢
⎢
( 1 − ϕp) + 3ϕp ∫ ( ) ⎥
kcl rcl + 2kbf ⎧ 2⎫
⎪ ⎡ ln( r / r¯ ) ⎤ ⎪
0 1 cl cl
keff =⎢ ⎥ kbf , n( rcl ) = exp⎨ −⎢ ⎥ ⎬
kbf n ( rcl) ⎪ ⎣ 2π ln σ ⎦ ⎪
⎢
( 1 − ϕp) + 3ϕp kcl( rcl) + 2kbf ⎥⎥
r 2π ln σ
⎩ ⎭
⎢
⎣ ⎦
⎡ k + 2k + 2 – –
28. Xuan et al. [131]
keff = ⎢
p bf ( kp − kbf ) ϕp ⎤⎥ k + ρpϕpcv,p KBT
⎢⎣ kp + 2kbf − ( kp − kbf ) ϕp ⎥⎦ bf 2 3π aclμ
29. Sabbaghdazeh and Ebrahimi [138] keff = kbf ⎡⎣ 1 − ϕp( 1 + M′)⎤⎦ + ϕp kp + klr M′ + ϕp ( 1 + M′) ⋯ – –
( )
abf
)( )
× 0.35 + 0.56Re0.3
bf
0.3k
Prbf bf
(
Pr 2ap + δ
⎡⎛ ⎞2 ⎤
M′ = ⎢ ⎜ + 1⎟ − 1⎥
δ
⎢ ⎝ ap ⎠ ⎥
⎣ ⎦
30. Pang et al. [140] ⎧ 0.1 Spherical
⎪ (
φp kp − kbf )
⎨1 +
⎪
⎩ ( ) ( )
1 − φp / n kp − kbf + kbf
(
+ A1 ln A2 φpRem
a Pr
0.3
⋯ ) Non-spherical
⎡ 1 + 2φ + 2
A3 ⎢
p ( 1 − φp) λ ⎤⎥⎫⎬ k
⎪
⎢⎣ 1 − φp + ( 2 + φp)λ ⎥⎦⎭ b ⎪
In the last few decades, research on nanofluids focused pri- 2.4.3. Effect of particle size
marily on thermal conductivity measurements alone, yet viscosity Observed fluctuation in viscosity of nanofluids has been at-
of the fluid is equally important and needs to be investigated tributed by researchers to particle size effect or magnitude of ag-
thoroughly [35,31]. Studies show the dependence of viscosity on gregates in the system [97,153,159–162]. However, quite a number
several system parameters such as temperature, volume con- of reports on particle size effects are conflicting. He et al. [97] in-
centration, particle shape, particle size, and pH among others. vestigated the rheological characteristics of Al2O3/water nanofluid
with particle sizes of 95, 145, and 210 nm. They concluded that the
2.4.1. Effect of particle volume concentration viscosity of nanofluids increases with particle size. Nguyen et al.
Most research works presented the variation of nanofluid [153] observed greater viscosities with 47 nm Al2O3 particles
viscosity with particle volume concentration [62,72,79,86,93,153– compared to values with 36 nm, especially at higher concentra-
157]. Nguyen et al. [153] observed the viscosity enhancement of tions. No significant effect on the size of the particles was observed
Al2O3(47 and 36 nm)/water at 23 °C to be 27% and 44% respec- by them at low concentrations. In contrast, Namburu et al. [159]
tively at 3% volume concentration. Williams et al. [86] showed that demonstrated that the viscosity of SiO2/60:40 ethylene glycol-
the viscosity of Al2O3(46 nm)/water increased by 14.7% at 3.0% vol. water decreases with the increase in the particle sizes of 20, 50
concentration. A similar observation on the viscosity increase with and 100 nm. Similar observation has been made by Lu and Fan
concentration has been made by Wang et al. [62], Lee et al. [154], [160] with Al2O3 (35, 45, and 90 nm) and Pastoriza-Gallego et al.
[161] with CuO (11 and 33 nm) water based nanofluids. However,
and Murshed et al. [93], etc. with of Al2O3/water, Kang et al. [72],
based on experiments with Al2O3 (27 and 40 nm) in propylene
Ferrouillat et al. [74], and Nikkam et al. [156], etc. with SiO2/water,
glycol (PG), Prasher et al. [162] observed the nanofluid viscosity to
Azmi et al. [155], Saleh et al. [79], and Jalal et al. [157], etc. with
be independent of particle size. It is apparent that contradictions
TiO2/water nanofluids respectively.
exist amongst the investigators regarding the effects of particle
size on the nanofluid effective viscosity . Such discrepancies
2.4.2. Effect of temperature
emanate mostly from experimental procedures and complexities
Temperature dependence of viscosity is a critical feature for the
in instrument calibration. Hence repeatability of experimental
effective utilization of nanofluids. The viscosity is expected to
measurements of nanofluids with viscosity values of other in-
decrease on exposure to high temperature fields due to weak in-
vestigators need to be ensured along with careful monitoring of
termolecular forces of attraction between the nanoparticles and
the size distributions at all volume fractions [32].
base fluid interface. Thus, the use of nanofluids at moderate par-
ticle loadings would be advantageous in applications involving
2.4.4. Effect of particle shape
high temperature build up [35]. The shape of the nanoparticles significantly influence the na-
Rheological studies undertaken by Anoop et al. [158] with nofluid viscosity which directly affect the heat exchanger pumping
Al2O3(50 nm)/water nanofluids for volume concentration o6.0% power requirement. Hence studies with different particle shapes
showed a decrease in viscosity with temperature in the range of on viscosity have been undertaken to achieve efficient and cost-
20–50 °C. Tavman et al. [71] observed the viscosity of SiO2(12 nm)/ effective cooling media. Jeong et al. [163] observed 77% viscosity
water at 4.0% vol. to decrease by 40% when the temperature in- enhancement with rectangular shaped ZnO/water particles of ag-
creased from 20 to 50 °C. Nguyen et al. [153] observed a reduction gregate size distribution of 150–370 nm compared to that of
in viscosity of CuO(36 nm)/water at 1.0% vol. concentration by 50% spherical particles in the size distribution of 57–150 nm at 5.0%
in the temperature range of 22–60°C. Namburu et al. [159] ob- volume concentration. Ferrouillat et al. [164] observed the visc-
served a similar trend with ethylene glycol water mixtures, where osity of rod-shaped ZnO/water nanofluid to be lower than with
the effective viscosity of CuO(29 nm)/60:40 EG-water nanofluid, polygonal shape particles. According to Timofeeva and co-workers
decreased significantly when subjected to heating in the tem- [87], the viscosity of nanofluid was greater with elongated
perature range of 35–50°C. Al2O3(80 10 nm)/50:50 ethylene glycol-water nanofluid as
664 S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678
Table 6
Empirical models for thermal conductivity.
B = 247.8, C = 140
μ ρbf VBrdp Kb T
Pr = , Re = , VBr = , μbf = A⋅10 B / (T − C ) , A = 2.414 × 10−5,
ρbf α μ 3πμ dplbf
B = 247.8, C = 140
47. Khanafer and Va- ⎡ 0.0235 Al2O3–W, CuO–W 11–150 0–10 20–70
⎛ 1 ⎞0.2246⎛ μeff ( T ) ⎞ ϕp2
keff = ⎢⎢ 0.9843 + 0.398 ϕp0.7383 ⎜ ⎟
ϕp
fai [38] ⎜ ⎟ ⋯× 3.9517 + 34.0341
⎝ dp ⎠ ⎝ μf ( T ) ⎠ T T3
⎣
ϕp ⎤
+ 32.509 ⎥ kbf
T2 ⎥
⎦
μf (T ) = 2.414 × 10−5 × 10247.8/ ( T − 140)
48. Patel et al. [66] ⎡ ⎛ k ⎞0.273 0.467 0.547 ⎛ 100 ⎞0.234 ⎤⎥ Al, Al2O3, Cu, CuO, TiO2/– 11–150 0–10 20–70
keff = ⎢ 1 + 0.135 ⎜ b ⎟ ( )T
ϕ ⎜ ⎟ k W, EG
⎢ ⎝ kp ⎠ 20 ⎝ dp ⎠ ⎥ bf
⎣ ⎦
49. Corcione [27] ⎡ ⎛ T ⎞10⎛ kp ⎞0.03 0.66⎤⎥ 2ρbf KbT
Al2O3, CuO, Cu, TiO2/–W, 10–150 0–9 20–50
keff = ⎢ 1 + 4.4 Re0.4Pr0.66 ⎜ ⎟ ⎜ ⎟
( ϕp )
k , Re = EG
⎢ ⎝ T fr ⎠ ⎝ kbf ⎠ ⎥ bf πμ 2 dp
⎣ ⎦ bf
50. Sharma et al. [26] ⎡ 1.37 0.2777 ⎛ dp ⎞
−0.0.336 ⎛ αp ⎞0.01737⎤⎥ Al2O3, CuO, TiO2, SiO2, 20–150 0–4 20–70
keff = ⎢ 0.8938 (1 + ϕ ) (1 + ) T
⎜1 + ⎟ ⋯× ⎜ ⎟ k Fe2O3, ZrO2, ZnO/–
⎢⎣ p 70 ⎝ 150 ⎠ ⎝ αbf ⎠ ⎥ bf
⎦
MWCNT– Multi-Walled Carbon Nanotube, EO–Engine Oil, EG–Ethylene Glycol, W–water, ND–Nanodiamond, HTO–Heat Transfer Oil, MO–Mineral Oil
compared to similar nanofluid system containing spherical shaped the particles incur additional stress on the nanofluid system. As a
particles of 9 nm diameter, for the same volume concentration. result, particles of large aspect ratio become dominant within the
In view of the observations made by the investigators, ag- fluid because of their greater surface area resulting in viscosity
gregate structures formed due to asymmetric bonding between increase.
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 665
Fig. 3. Single spherical particle with interfacial layer in a fluid medium. Leong et al. Fig. 5. Modes of energy transport in nanofluids (particle dynamic effect). Jang and
[114]. Choi [101].
Fig. 7. Comparison of thermal conductivity ratio of single material CuO nanofluid Fig. 9. Comparison of thermal conductivity ratio of single material TiO2 nanofluid
Eqs. (49) and (50) at different particle volume concentrations. with Eqs. (49) and (50) at different particle volume concentrations.
(120) and experimental data of Kang et al. [72] and Azmi et al.
[155] for SiO2(17 and 22 nm)/water respectively is shown in Fig. 11.
The experimental data of SiO2/(17 nm) deviate from the predicted
values of Eqs. (119) and (120) by 8.8% and 6.4% respectively, while
the deviation is 3.2% and 1.7% with SiO2 (22 nm) in the con-
centration range of 0–5% vol. concentration. Summary of the
comparisons of the viscosity predictions with regression Equations
(119) and (120) has also been given in Table 10.
It is observed that the values of viscosity estimated with Eqs.
(199) and (120) do not deviate by more than 20% for most of the
nanofluids reported in the literature. Therefore, Eqs. (119) and
(120) are further extended to the estimation of composite nano-
fluid viscosity.
Table 7
Summary of thermal conductivity validation for single material nanofluid.
S. No. Nanofluid Reference ϕ T dp Kr (Exp.) Kr Eq. (49) (Corcione)[27] Kr Eq. (50) Sharma)[26]
( )
ρnf = 1 − ϕp ρnf + ϕp, 1
ρ1 + ϕp, 2
ρ2 (122)
cnf =
(1 − ϕ ) ρ
p
c
nf bf
+ ϕp,1 ρ1cp,1 + ϕp, 2
ρ2 cp,2
ρnf (123)
where ρ1 and ρ2 are the densities of individual nanoparticles
3.2. Specific heat of composite nanofluid 3.3. Thermal conductivity and Viscosity of composite nanofluid
The nanofluid specific heat given by Eq. (3) applicable for SmNf Two models for the estimation of thermal conductivity (49),
is in good agreement with the experimental data as shown in (50) and viscosity (119), (120) of SmNf have been presented. It can
Fig. 5. Hence the equation for the specific heat of SmNf is reported be observed that thermal conductivity and viscosity of SmNf is
to be applicable by Takabi et al. [221] based on the law of mixtures dependent on concentration, particle size and temperature. In
given by: addition, the thermal conductivity is dependent on the material
668 S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678
Table 8
Theoretical viscosity models.
+( 1155
128
+
935
96
β +
235 3
96
β + β )ϕ
5 4
48
4
p
⎤
+( )ϕ
3003 1125 1465 2 95 3 1 4 5
+ β + β + β + β p + ⋯⎥⎦ μbf
256 64 192 96 48
75 Chen et. al. [191] ⎡ ⎛ −[ η] ϕp, max ⎤ – Spherical
aa 1.2⎞
μeff = ⎢ ⎜ 1 − ⎥μ
ϕa
⎢ ⎝
⎣
ϕp, max ( )
a
⎟
⎠ ⎥ bf
⎦
⎡ –
76. Brouwers [192]
⎢ ⎛ 1 − ϕp ⎞bϕp, max / ( 1−ϕp, max)⎤⎥ 0.64
μeff =⎢ ⎜ ⎟ ⎥ μbf
⎢⎣ ⎝ 1 − ϕp / ϕp, max ⎠
⎥⎦
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 669
Table 9
Theoretical viscosity models.
77. Tseng and Lin [193] μeff = ⎡⎣ 13.47 exp ( 35.98) ϕp⎤⎦ μbf TiO2–W 7–20 0–0.12 20–30
1 1 1
78. Maiga et al. [194] 1
μeff = ⎡⎣ 1 + 7.3 ϕp + 123 ϕp2 ⎤⎦ μbf Al2O3–W 13, 28 0–5 25
2 2
2
μeff = ⎡⎣ 1 − 0.19 ϕp + 306 ϕp2 ⎤⎦ μbf Al2O3–EG 28
1 1
79. Buongiorno [195] 1
μeff = ⎡⎣ 1 + 39.11 ϕp + 533.9 ϕp2 ⎤⎦ μbf Al2O3–W, 13, 227 0–10 25
2
TiO2–W
2
μeff = ⎡⎣ 1 + 5.45 ϕp + 108.2 ϕp2 ⎤⎦ μbf
80. Prasher et al. [162] Al2O3–PEG 27, 40, 50 0–3 30–60
(
μeff = 1 + 10 ϕp μbf )
81. Chen et al. [191] μeff = ⎡⎣ 1 + 10.6 ϕp + 10.6 ϕp2 ⎤⎦ μbf TiO2–EG 25 0–3 20–50
1,3 1
82. Nguyen et al. [153] 1
μeff = ⎡⎣ 1 + 0.025 ϕp + 0.015 ϕp2 ⎤⎦ μbf Al2O3–W 36,347, 2
1–9.4 20–75
29
2
μeff = ⎡⎣ 1.475 − 0.319 ϕp + 0.051 ϕp2 + 0.009 ϕp3 ⎤⎦ μbf
3
3
μeff = ⎡⎣ 0.904 exp ( 0.148) ϕp ⎤⎦ μbf CuO–W
1 1
83. Williams et al. [86] 1
⎡ 4.91 ϕp ⎤ Al2O3–W, 46, 260 1
0–3.6 20–80
μeff = exp⎢ ⎥μ 2
ZrO2–W 2
0–9
⎣ 0.2092 − ϕp ⎦ bf
2
⎡ 11.19 ϕp ⎤
μnf = exp⎢ ⎥μ
⎣ 0.1960 − ϕp ⎦ bf
1 1,2 1
84. Rea et al. [196] ⎡ ⎤ Al2O3–W, 50 0–6 20–80
1
(
μeff = ⎣ exp 4.91 ϕp /0.2092 − φp ⎦ μbf )
2 2
2
μeff = ⎡⎣ 1 + 46.80 ϕp + 550.82 ϕp2 ⎤⎦ μbf ZrO2–W 0–3
1
85. Duangthongsuk and 1
μeff = 1.0226 + 0.0477ϕp − 0.0112 ϕp2 TiO2–W 21 0.2–2 15, 225,
3
Wongwises [67] 35
2
μeff = 1.0113 + 0.0920 ϕp − 0.015 ϕp2
3
μeff = 1.0180 + 0.0112 ϕp − 0.0177 ϕp2
86. Godson et al. [148] μeff = ⎡⎣ 1.005 + 0.497 ϕp − 0.1149 ϕp2 ⎤⎦ μbf Ag–W 60 0.3–0.9 50–90
c 3 c,d,e
SiO2/ 0–0.1
( A = 1.0920, B = 5.9540)
3,1 3,1
d –EG/W
( A = 0.9693, B = 7.0740)
3,2 3,2
e
( A = 1.0050, B = 4.6690)
3,3 3,3
Table 9 (continued )
4 4
A = 1.98752, B = 0.01128
4
5
A = 2.13350, 5
B = 0.00999 0–0.01
5
0–0.015
98. Kole and Rey [204] B CuO–Gear oil 40 0–2.5 10–80
( )
log μeff = A + 1000
( T + C)
1 1 1
A = − 0.70784, B = 0.70912 C = − 171.049
2 2 2
A = − 1.11379, B = 1.23013 C = − 104.976
3 3 3
A = − 4.94087, B = 3.37827 C = − 26.2139
4 4 4
A = − 1.10774, B = 1.43086 C = − 87.08024
99. Kulkarni et al. [205] CuO–W 29 5–15 5–50
( )
ln μeff = A⋅ ( )−B
1
T
ϕp ϕp2 ϕp ⎤
−8.11 −
27463.863
+ 0.0127 ϕp3 + 1.6044 + 2.175 ⎥
T˜ T˜ ⎥
3 T˜ 2
T˜ ⎦
⎡ Al2O3–W
106. Masoud Hoseini
et al. [210]
⎛ T⎞
μeff = exp⎢ m + α ⎜ ⎟ + β ϕh + γ
⎣ ⎝ T0 ⎠ ( ) ( )⎤⎥⎦ μ
d
1+r bf
36, 47 1.0, 4.0 20–65
⎛ dp + 2s ⎞3
ϕh = ϕp ⎜ ⎟ , m = 0.72, α = − 0.485, β = 14.94, r = 1, s = 2.5,
⎝ dp ⎠
o
To = 20 C
107. Khanafer and Vafai ⎡ ϕp TiO2–W 27 0.9, 2.0, 3.1 20–70
μeff = ⎢ 0.6002 − 0.5690 ϕp + 0.0823 ϕp2 + 28.8763 ⋯
[38] ⎣ T
ϕp2 ϕp2 ⎤
− 204.2202 + 561.3175 ⎥μ
T2 ⎥
bf
T2 ⎦
108. Khanafer and Vafai ⎡ 8.4312 524.7147 ϕp CuO–W 29 1–9.4 20–75
μeff = ⎢ −0.4262 + + 0.898 ϕp + − 0.2217 ϕp2−4.7329
[38] ⎣ T T2 T
ϕp2 ϕp ⎤
+70.3105 + 0.0176 ϕp3 − 5559.4641 ⎥ μbf
T2 T3 ⎥
⎦
109. Khanafer and Vafai ϕp ϕp2 Al2O3–W 13 1.34, 2.78 20–70
[38] μeff = 0.4444 − 0.254 ϕp + 0.0368 ϕp2 + 26.333 − 59.311
T T2
110. Khanafer and Vafai ⎡ 18.0162 164.0837 ϕp Al2O3–W 36 1–9.1 20–70
μeff = ⎢ −0.1011 − + 0.3619 ϕp + − 0.0966 ϕp2+0.1609
[38] ⎣ T T2 T
ϕp2 ϕp ⎤
+ 22.4901 + 0.0078089 ϕp3 − 2316.3754 ⎥ μbf
T2 T3 ⎥
⎦
111. Khanafer and Vafai ⎡ ϕp ϕp2 Al2O3–W 47 1–9.4 20–70
26.9036 24.114
[38] μeff = ⎢ −0.4892 − + 0.6837 ϕp + − 0.1785 ϕp2+0.1818 + 27.015
⎣ T T2 T T2
ϕp ⎤
+ 0.0132 ϕp3 − 2940.1775 ⎥ μbf
T2 ⎥
⎦
112. Khanafer and Vafai μeff = ⎡⎣ 1.0538 + 0.1448 ϕp − 3.363 × 10−3T − 0.0147 ϕp⋯ Al2O3–W 21 0.2–2 15–35
[38]
ϕp ⎤
+ 6.735 × 10−5T 2−1.337 ⎥μ
T ⎦ bf
Table 9 (continued )
ϕp ϕp2 ϕp3 ⎤
− 2354.7358 + 23.498 − 3.0185 ⎥μ
T3 2 2 ⎥ bf
dp dp ⎦
Fig. 10. Comparison of single material CuO nanofluid viscosity with Eqs. (119) and
Fig. 11. Comparison of single material SiO2 nanofluid viscosity with Eqs. (119) and
(120) at different temperatures.
(120) at different particle volume concentrations.
Table 10
Summary of viscosity validation for single material nanofluid.
S. No. Nanofluid Reference ϕ Temperature (°C) dp μnf (Exp.) μnf (Sharma)[119] μnf (Corcione)[120]
Fig. 12. Prediction of composite nanofluid density with Eq. (122) for different Fig. 13. Prediction of composite nanofluid specific heat with Eq. (123) for different
particle volume concentrations. particle volume concentrations.
S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678 673
Fig. 16. Prediction of composite nanofluid effective thermal conductivity ratio with
Fig. 14. Comparison of composite nanofluid effective thermal conductivity ratio
Eqs. (49) and (50) at different mixing proportions and temperatures.
with Eqs. (49) and (50) at different particle volume concentrations.
Fig. 17. Prediction of composite nanofluid effective thermal conductivity ratio with
Eqs. (49) and (50) at different ratios, different particle sizes and temperatures.
Fig. 15. Comparison of composite nanofluid effective thermal conductivity with
Eqs. (49) and (50) at different particle sizes and volume concentrations.
1.0–5.0% vol. concentration compared to values of 40:60 evaluated
concentration. The specific heat decreases with concentration for at a temperature of 25 °C. It is observed that an increase in the
all composite nanofluids. The values of specific heat with 60% SiO2 proportion of the SiO2 mixture ratio from 40% to 60% by weight
weight ratio is greater than with 40% weight ratio for any com- does not influence significant variation in the overall thermal
posite material. It can be observed that the specific heat of Ag, CuO conductivity of CNf especially in predicting values using Eq. (49)
and Al2O3 is lower for SiO2 material. Hence higher ratio of SiO2 than with Eq. (50). This is due to lower values of thermal con-
(60%) predict greater values of nanofluid specific heat compared to ductivity of SiO2 in comparison to Ag and Al2O3. The result shows
values with 40% for any CNf. that greater thermal conductivity of a material has a dominant
The variation of thermal conductivity with concentration for influence on composite nanofluid value than with materials hav-
two CNfs is shown through Figs. 14 and 15. The experimental data ing lower values of kp. Eq. (49) predicts higher values of nanofluid
of Suresh et al. [219] and Madhesh et al. [17] displayed in Fig. 14 thermal conductivity compared with large sized particles. The
departed from the values estimated with Eqs. (49) and (50) of thermal conductivity with particles of equal size viz., 20:20 nm
Corcione [27] and Sharma et al. [26] by maximum deviation of predict higher thermal conductivity in comparison with particles
18.3% and 7.0% respectively. A satisfactory agreement of the ex- of size 60:20 nm by an average value of 3.0%.
perimental data of Hemmat Esfe et al. [220] with the predicted The effect of temperature on thermal conductivity of CNf hav-
values estimated using Eqs. (49) and (50) can be observed from ing 60:40 mixture ratio for two particle sizes and composite ma-
Fig. 15. The deviation of the experimental data with the predicted terials is shown in Fig. 17. It can be observed that the thermal
values is within þ8% and 8% respectively. conductivity of CNf increases with temperature and decreases
The predicted value of thermal conductivity with 60:40 mix- with particle size. The predicted values with smaller size particle
ture ratio shown in Fig. 16 is greater in the concentration range of of Ag (20 nm) is greater when compared to Al2O3 (60 nm) for a
674 S. Akilu et al. / Renewable and Sustainable Energy Reviews 66 (2016) 654–678
Fig. 20. Prediction of composite nanofluid effective viscosity ratio with Eqs. (119)
Fig. 18. Comparison of composite nanofluid effective viscosity with Eqs. (119) and
and (120) at different particle volume concentrations and temperatures.
(120) at different particle volume concentrations.
5. Conclusions
Acknowledgment
constant particle size of SiO2 (20 nm). The deviation in the values
estimated with Eqs. (49) and (50) is about 1.1%.
A comparison of experimental values of CNf viscosity with The authors would like to extend their appreciation to MOE
computed values using Eqs. (119) and (120) of Sharma et al. [26] Malaysia for financial support (Grant No.: FRGS/1/2014/TK01/UTP/
and Corcione [27] respectively is shown in Fig. 18. A satisfactory 01/1) and Universiti Teknologi PETRONAS (UTP) for proving facil-
agreement of the experimental data of Hemmat Esfe et al. [220] ities for the conduct of research.
with the values estimated with the equations can be observed.
However, the deviation of the experimental data of Suresh et al.
[219] could not be explained. References
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