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Article history: The experimental data on the viscosity and thermal conductivity (TC) of ethylene glycol (EG)-based hybrid
Received 31 July 2018 nanofluids (HyNFs) dispersed with a SiC–CuO/C nanocomposite (NC) is reported for the first time. The rheolog-
Received in revised form 10 February 2019 ical behavior and dynamic viscosity have been analyzed with a computer controlled rotational rheometer over a
Accepted 25 April 2019
temperature range from 298.15–353.15 K and shear rate from 20 to 200 s−1. The TC was measured using tran-
Available online 29 April 2019
sient hot-wire method for NF concentrations up to 3.13 wt%. The effect of the temperature and volume fraction
Keywords:
of the nanoparticles (NPs) on the thermophysical properties were examined under atmospheric pressure. The
SiC experimental findings revealed that the TC increases with the concentration and temperature, while the viscosity
CuO/C increases with concentration and decreases with temperature as expected. HyNF exhibit substantially higher TC
Ethylene glycol and viscosity enhancement compared to single-particle based NF under similar conditions. The enhanced prop-
Thermal conductivity erties of the HyNF could be attributed to the synergetic effects of the composite particles and the underlying
Viscosity physical mechanism in the fluid medium. The existing theoretical models failed to predict the experimental
Hybrid nanofluid data. Herein, a new correlation is presented as a function of concentration and temperature for the TC and
viscosity.
© 2019 Elsevier B.V. All rights reserved.
https://doi.org/10.1016/j.powtec.2019.04.061
0032-5910/© 2019 Elsevier B.V. All rights reserved.
S. Akilu et al. / Powder Technology 354 (2019) 540–551 541
size exhibited larger TC enhancement values up to 20%. Żyła and Fal [8] temperature on TC of SiC (30 nm) NFs was presented by Li et al. [15].
prepared SiO2 (7–14 nm) NFs and measured the TC at 298 K for a sam- Approximately TC improve up to 16.2% of NFs was found in the study.
ple with 2.6% vol. The result showed that using NF enhanced the TC by Enhancement in TC was approximately 23% over that of EG at 1.0 vol%
3.3% compared to pure EG. Murshed et al. [9] observed about 18% ad- in the temperature range of 293–323 K. Additionally, the Maxwell
vance in TC of EG at about 5.0 vol% of TiO2 (15 nm) NPs. Longo and model presented by the authors is unable to correlate the experimental
Zilio et al. [10] reported the increase in TC of the TiO2 (15 nm)/EG at data. Many other findings on TC of EG-based NFs have been reported
3.0% volume fraction was about 19.5% at 323 K. Xie et al. [11] dispersed using a variety of nano-additive materials [16–25]. Nevertheless, from
MgO particles of mean diameter 20 nm in EG with different concentra- a practical point of view, when NPs are added in a base liquid, in addi-
tions (0.5–5.0)% vol. The TC of the NF improved by 40.6% at 303 K. They tion to the viscosity fluctuations the rheological properties change too,
opined that bulk material TC, particle size, nanoparticle Brownian mo- hence researchers have simultaneously inspected these phenomena.
tion, nanolayering, clustering, and viscosity are possible factors respon- Experimental investigation of SiO2 particles as dispersed additives to
sible for the augment of TC of NFs. According to the study done by EG has been performed by Akilu et al. [26]. The results showed that, at
Moosavi et al. [12], the TC of EG can be enhanced by 10.5% with ZnO the same volume concentration and temperature, the viscosity of base
(67 nm) dispersion in the presence of ammonium citrate as a stabilizer. liquid EG was lower than that of SiO2 NFs. The viscosity of pure EG
Xie et al. [13] reported the TC behavior of EG using different particle was enhanced by 39% when it was mixed with SiO2 NP as reported in
sizes of SiC (26 and 600 nm), up to 13 and 23% of enhancements were the study by Żyła and Fal [8]. Furthermore, it was noted from the previ-
found at a low temperature of 277 K. Bobbo et al. [14] examined the ef- ous paper [27] that temperatures, particle concentrations, and aggrega-
fect of temperature on the TC of SiC (10–50 nm)/EG NF with various tion had a substantial influence on the viscosity of EG-based NFs. The
weight concentrations 0.1, 1.0, and 5.0 wt%, in temperature range effect of adding SiC particles on the rheological behavior of EG suspen-
from 283 to 343 K. They showed that, for maximum concentration, a sion was explored by Li et al. [28]. The results revealed that the viscosity
rise of the temperature causes the increase TC of suspension from 12 of the suspensions increases with the loading of the NPs. They also
to 21%. Also, another result obtained from experiments on impacts of found the NF behaving as a shear thinning at the low shear rates and
Table 1
Summary of previous studies on thermal conductivity of EG-based nanofluids.
Material Base liquid NF synthesis method Particle loading Particle diameter Temperature TC enhancement Ref.
Single-NPs
Ag EG Two-step 0.1–2.0 vol% 12 nm 303–368 K ~2% Madhesh et al. [6]
Ag EG Two-step 0.027–0.107 vol% 7.3 nm 293–313 K 10% Seyhan et al. [16]
AiN EG Two-step 1.8–7.9 vol% 20 nm 298 K 21.7% Żyła and Fal et al. [19]
Al EG Two-step 1.0–5.0 vol% 80 nm 294–333 K 45% Murshed et al. [9]
Al2O3 EG Two-step 1.0–5.0 vol% 38 nm 293 K 18% Lee et al. [7]
Al2O3 EG Two-step 1.0–5.0 vol% 10 nm 273–323 K 29.1% Longo and Zilio [10]
CuO EG Two-step 1.0–4.0 vol% 23 nm 293 K 20% Lee et al. [7]
Gr EG Two-step 0.07% 5 nm 303–323 K 37% Van Trinh et al. [21]
Gr EG Two-step 0.005–0.03 vol% Nonea 298–323 K 7% Baby and Ramaprabhu [22]
MgO EG Two-step 0.5–4.0 vol% 20 nm 283–333 K 40.6% Xie et al. [11]
SWCNH EG Two-step 0.1–1.5 vol% 2–5 nm 298 K 11% Selvam et al. [23]
SWCNT EG Two-step 0.5–2.5 vol% 1–4 nm 298–323 K 38% Amrollahi et al. [20]
SWCNT EG Two-step 0.03–0.21 vol% 1 nm 298 K 14.8% Harish et al. [24]
MWCNT EG Two-step 0.07% 10–30 nm 303–323 K 21% Van Trinh et al. [21]
MWCNT EG Two-step 0.04 vol% Nonea 298 K 7.3% Jha and Ramaprabhu [25]
ND EG Two-step 0.32–3.38 vol% 4 nm 298 K 4.9% Żyła et al. [17]
SiC EG Two-step 0.8–4.3 vol% 26 nm 277 K 13.5% Xie et al. [13]
SiC EG Two-step 0.8–4.3 vol% 600 nm 277 K 23% Xie et al. [13]
SiC EG Two-step 0.1–5.0 wt% 10–50 nm 283–343 K 21% Bobbo et al. [14]
SiC EG Two-step 0.5–1.0 vol% 30 nm 293–323 K 23% Li et al. [15]
SiO2 EG Two-step 0.5–2.6 vol% 7–14 nm 298 K 3.3% Żyła and Fal et al. [8]
SiO2 EG Two-step 0.5–2.0 vol% 21 nm 303–333 K 11.5% Akilu et al. [26]
TiN EG Two-step 0.22–1.18 vol% 20 nm 298 K 6.03% Żyła et al. [18]
TiN EG Two-step 0.22–1.18 vol% 50 nm 298 K 4.92 Żyła et al. [18]
TiO2 EG Two-step 1.0–5.0 vol% 15 nm 294–333 K 18% Murshed et al. [9]
TiO2 EG Two-step 1.0–3.0 vol% 15 nm 273–323 K 19.5% Longo and Zilio [10]
ZnO EG Two-step 1.0–3.0 vol% 67.1 nm 283–333 K 10.5% Moosavi et al. [12]
Composite-NPs
Ag-Gr EG Two-step 0.001–0.07 vol% 10 nm 298–343 K 14% Baby and Ramaprabhu [34]
Ag-MWCNT EG Two-step 0.012–0.03 vol% 10–20 nm 303–322 K 29.03% Jha and Ramaprabhu [25]
Al-Zn EG Two-step 0.01–0.1 vol% 15 nm 303–343 K 16% Paul et al. [30]
Au-MWCNT EG Two-step 0.006–0.024 vol% 10–20 nm 303–322 K 27% Jha and Ramaprabhu [25]
Cu-MWCNT EG Two-step 0.008–0.04 vol% 3–30 nm 303–322 K 20.2% Jha and Ramaprabhu [35]
CuO-Gr EG Two-step 0.007–0.01 vol% 8.5 nm 298 K 28% Baby and Sundara et al. [36]
Fe3O4-MWCNT EG Two-step 0.1–2.3 vol% 5–30 nm 298–323 K 30% Harandi et al. [38]
Gr-CNT EG Two-step 0.0175–0.07 vol% 3–30 nm 303–322 K 50% Van Trinh et al. [21]
Gr-MWCNT EG Two-step 0.011–0.04 vol% 2–19.2 nm 298–323 K 24% Aravind and Ramaprabhu [39]
MgO-MWCNT EG Two-step 0.05–0.6 vol% 5–40 nm 298–323 K 21.3% Afrand et al. [37]
ND-Co3O4 EG Two-step 0.05–0.15 wt% 16.9 nm 293–333 K 8.7% Sundar et al. [33]
ND-Ni EG Two-step 0.62–3.03 wt% 30 nm 293–333 K 13% Sundar et al. [41]
Pd-MWCNT EG Two-step 0.06–0.03 vol% 10–20 nm 303–322 K 17.34% Jha and Ramaprabhu [25]
TiO2-CuO/C EG Two-step 0.5–2.0 vol% 24 nm 303–333 K 16.7% Akilu et al. [31]
SiO2-MWCNT EG Two-step 0.05–1.95 vol% 5–30 nm 298–323 K 22.2% Hemmat-Esfe et al. [40]
ZnO-TiO2 EG Two-step 0.1–3.5 vol% 30–45 nm 298–323 K 32% Toghraie et al. [32]
a
Not cited information.
542 S. Akilu et al. / Powder Technology 354 (2019) 540–551
2. Experimental
2.1. Materials
Silicon carbide (SiC) NPs (Beta, 99% pure, 45–65 nm nominal diam-
eter, density 3216 kg m−3) were supplied by US Research
Nanomaterials Inc., USA. n-Hexane (H) was acquired from ACROS
Table 2
Pertinent property of used materials for nanofluid synthesis.
SiC CuO/C EG
Fig. 3. Experimental measurement setup (a) thermal conductivity (b) Rheological and viscosity.
544 S. Akilu et al. / Powder Technology 354 (2019) 540–551
Fig. 4. TEM images of NPs (a) SiC (b) CuO/C and (c) SiC-CuO/C nanocomposite.
dispersion technique ideally for non-inert, non-functionalized colloidal the size measurements were performed at 298 K with a scattering
materials [50]. The success of this process is that no direct molecular in- angle of 173°.
teraction would occur between the ultrasound and the dispersion [52]. The thermal conductivity measurements were performed according
In this work, a probe sonication system has been employed as illustrated to the transient hot-wire technique at atmospheric pressure using a
in the schematic diagram of Fig. 2. Pohl and Schubert [53] reported that thermal property analyzer (KD2 Pro, Decagon Devices Inc., USA). This
the de-agglomeration rate is independent of the solid concentration up device was equipped with a KS-1 probe sensor (60 mm long, 1.3 mm di-
to 50% weight loading. Thus, the optimum loading of composite NPs was ameter). The needle probe served both as a temperature sensor and line
fixed at 3.13 wt%. Sample temperatures throughout the sonication pro- heat source for the thermal conductivity determination in the range of
cess were controlled in an ice-water bath to minimize overheating. For 0.2–2.00 W m−1 K−1. A 50 ml sample was filled into a glass vial and
the preparation of 55 ml NF samples, the designated particle concentra- sealed with a silicon septum cover. The KS-1 probe was inserted verti-
tions 0.82, 1.62, 2.42, and 3.13 wt% were evaluated according to the mix- cally into the vial through the center of the septum. The assembly of
ture rule formula given the Eq. (1) the vial and the probe was then immersed in a thermostatic water
mSiC−CuO=C
φm ¼ 100 ð1Þ
mSiC−CuO=C þ mEG
Element Atomic%
and the equivalent concentrations of the NF in percentage by volume CK 42.09
were found to be 0.25, 0.51, 0.77, and 0.99%, respectively. OK 48.89
The pH values of the NF samples were measured using a pH meter
(FiveEasy FE 20, Mettler Toledo, Switzerland) which had shown values Si K 8.66
ranging between 5 and 6. Furthermore, to keep away from the isoelec- Cu K 0.35
tric point for the SiC at pH ≈ 4.9 [54] where there is a high possibility
100
of electrostatic attraction amongst the NPs, the suspensions were ad-
justed to the pH value of 11 using a NaOH solution. The hydrodynamic
particle size and zeta potential measurements of the SiC-CuO/C EG NF
were determined by dynamic light scattering (DLS) using a zeta sizer
(Nano ZS, Malvern Instruments, UK) at a laser wavelength of 633 nm.
The zeta potential was measured using a Z-dip cell in Auto-mode. All Fig. 5. EDX spectra with the table of the detected elements.
S. Akilu et al. / Powder Technology 354 (2019) 540–551 545
The TEM analysis of the particles revealed that the SiC and CuO/C
were spherical NPs of loose agglomerates with average sizes of 29 nm
and 28.6 nm, respectively (Fig. 4a and b). The SEM image of the SiC-
CuO/C NP composite is depicted in Fig. 4(c). It could be seen that the
Fig. 6. XRD patterns (a) CuO/C (b) SiC and (c) CuO/C-SiC nanocomposite powders.
CuO/C NPs were homogeneously distributed within the SiC ensemble.
The inset represents the corresponding distribution histogram revealing
the average size of the composite particles.. Fig. 5 displays the scan of
bath (Vivo-RT2, Julabo-GmbH, Germany) maintained at a constant tem-
the EDX spectrum for the selected area in the SiC-CuO/C. The powder
perature with a precision of ±0.1 K. A series of calibrations of the sensor
was found to be composed of Si, C, O, and Cu elements in which no sig-
needle were undertaken by measuring the TC of EG as a standard sam-
nificant impurity from other elements could be spotted.
ple. The deviation of the measured TC from the reference data was about
The crystal structure analysis was performed by X-ray diffraction
±2% [55] as shown in Table 3(a). Suresh et al. [56] showed a deviation of
which is presented in Fig. 6. According to the XRD data as shown in
about 3% by comparison of their experimental data with the reference
Fig. 6 curve (a), the positions of the diffraction lines with (hkl) =
values for water. The data from Nabil et al.'s [57] study revealed the
(110), (002), (111), (202), (202), (113), (022), and (113) were attrib-
maximum deviation of ±1.6% from the reference values of the TC of
uted to the monoclinic copper phase according to the JCPDS data file
the EG/W mixture. In general, these results validate the operating pro-
#045–0937 [58]. No distinct peak for carbon was visible in the pattern
cedure employed and the reliability of the measurement. The TC was
due to its amorphous character. In Fig. 6 curve (b), the reflections of
then recorded under automatic mode time intervals of 15 min for 6 h
the pattern indicate the presence of the β-SiC phase, respectively
at a constant temperature in the range from 298.15 to 333.15 K. An av-
(JCPDS Card No. 01–074-2307), in agreement with the reported value
erage of at least 10 successive readings were considered in the process
of Nikkam et al. [59]. In addition, both the CuO and SiC peaks were
of establishing the final value.
strongly detected in the composite samples from the XRD patterns as
Rheological measurements were performed by using a modular
evidenced in Fig. 6 curve (c).
compact rotational rheometer (Physica MCR 302, Anton Paar, Austria).
Rotational and oscillatory measurements can be made using either a
double gap or cone or plate geometries. To provide accurate results, 3.2. Dispersion formula and stability
the double gap concentric cylinder geometry system (DG 26.7) for low
viscosity fluids was used for the study. About 10 ml of a sample was in- Fig. 7 shows the hydrodynamic size distribution of the HyNF samples
troduced into the double gap chamber. The measuring unit was secured prepared by using magnetic stirring and ultrasonication. The SiC-CuO/C
onto the rheometer in a horizontal orientation. The distance between NF prepared under 2 h magnetic stirring displayed a bimodal hydrody-
the double gap cylinders, one of which remained stationary and the namic particle size distribution, whereas a combination of magnetic
other of which rotated, was set to 1 mm. The measurement of the cell stirring and ultrasonic treatment for 2 h led to a single narrow distribu-
temperature was controlled by a built-in high accuracy Peltier thermo- tion peak. Obviously, the impact produced by the cavitation of the ultra-
stat with a precision of ±0.1 K. In order to check the proper operation sonic waves was responsible for reducing the agglomerate particles into
and accuracy of the measurements, the instrument was calibrated smaller sizes of monomodal distribution (531–895 nm). Furthermore,
with ethylene glycol as a standard solution. A good agreement between the hydrodynamic diameter of the NPs in the NF obtained by using
the reference and measured data was observed within a ± 5% deviation the DLS did not correlate with an average primary particle size of the
[55] as shown in Table 3(b). A similar validation performed by Nabil NC in accordance with the Stokes-Einstein equation. This is attributed
et al. [57] disclosed an acceptable consistency of the measured data to particle clusters and the adsorption effect of the NPs [56].
when compared with the literature data. After the calibration of the rhe- The stability of the NFs was determined using the zeta potential and
ometer system was complete, acquisition and determination of the sedimentation method. A suspension of absolute zeta-potential above
Fig. 7. Hydrodynamic particle size distribution by intensity for SiC-CuO/C hybrid nanofluid at 0.82 wt%, prepared by 2 h each for magnetic stirring and ultrasonic probe sonication methods.
546 S. Akilu et al. / Powder Technology 354 (2019) 540–551
30 mV is considered stable [60]. The measured zeta potential value for Table 4
the diluted NFs with particle concentrations of 0.82%, 1.62%, 2.42%, Dependence of thermal conductivity on particle concentration and temperature on ther-
mal conductivity of SiC-CuO/C nanofluid.
and 3.13 wt% were 45 mV, 42 mV, 40 mV, and 34 mV, which confirms
the acceptable stability of the suspension due to the stronger repulsion φm/wt knf/W·m−1·K−1
of the NPs at a pH value of 11. Fig. 8 depicts the photo of the SiC-CuO/C %
298.15 303.15 308.15 313.15 318.15 323.15 328.15 333.15
NF samples after a 30-day preparation time. No apparent disparity was K K K K K K K K
observed from the one taken immediately after preparation. In addition, 0.00 0.2511 0.2520 0.2534 0.2546 0.2552 0.2563 0.2571 0.2582
the changes in the cluster size distributions observed were very low 0.82 0.2613 0.2651 0.2683 0.2721 0.2742 0.2772 0.2813 0.2843
during the said period, which affirms the good dispersion stability of 1.62 0.2641 0.2673 0.2703 0.2741 0.2763 0.283 0.2851 0.2892
the NC. 2.42 0.2654 0.2682 0.2724 0.2772 0.2792 0.2851 0.2882 0.2951
3.13 0.2733 0.2771 0.2799 0.2854 0.2881 0.2954 0.2982 0.3081
3.3. Thermal conductivity of the SiC-CuO/C nanofluids The relative standard uncertainty of thermal conductivity is 2.0%.
The experimental data of the TC of the SiC-CuO/C composite NF with via the wet mixing technique, obtaining a 16.7% enhancement in the
particle concentrations and temperatures are presented in Table 4. The TC when dispersed in EG at 333.15 K. A TC enhancement of 32% with
results indicate that the TC of the HyNF increased with the concentra- ZnO–TiO2/EG at 323.15 K was reported by Toghraie et al. [32]. A signif-
tion and temperature. An increase in the NF concentration implies icantly higher enhancement of 40% was reported for Cu/TiO2-water/EG
that there was a greater number of particles in contact with the base liq- by Hemmat-Esfe [62] with 2.0% volume concentrations at 323.15 K. The
uid molecules. A large surface to volume ratio resulted in collisions and similar trend was found for the suspension of TiO2-SiO2/EG/W [57].
interactions between the particles leading to the enhancement in the In Fig. 10, the measured TC enhancement data of the HyNF in com-
thermal conductivity. Van Trinh et al. [61] described the behavior parison with the single-component particle NF are displayed. The rela-
based on the percolation phenomenon. It was explained that when tive TC of NFs was plotted for various particle concentrations. The
the volume fraction of NPs increases, the mean free path of the NPs percentage TC enhancements of the SiC to the SiC-CuO/C NF (kr,nf: kr,
will also increase. As a result, the frequency of the lattice vibration in- HyNF) for the 0.82 wt% concentrations were determined to be 1.9% and
creases which in turn enhances the TC that increases with temperature. 4.1%; whereas for the 3.13 wt%, the enhancement values were 5.5%
The main reason for the TC enhancement with temperature might be and 8.8%, respectively, at 298.15 K. Thus, the TC enhancement is nearly
due to the micro convection induced by the Brownian motion of the doubled for the HyNF compared to the single particle-based SiC NF. The
NPs. Moreover, the feeble increase of TC with temperature observed enhancement indicates the synergistic role of composite particles. It is
may be associated with high viscosity of the base liquid (EG). It is well well established that the TC of NFs depends on the physical properties
known that the pure glycol exhibits strong intermolecular forces due of the constituent materials. In view of that, substituting 20% by weight
to hydrogen bonds. This result in higher resistance to the motion of of the SiC (29 nm) in EG with an equal mass of CuO/C (20 nm) will in-
the fluid molecules and NPs. Besides that, an increase in the tempera- crease the number of particles, leading to a large solid surface area in
ture rises the average kinetic energy of the molecules, giving rise to the suspension. Botha et al. [63] reported that the TC of an oil-based
the breakdown of the intermolecular forces. As viscosity decreases, the NF was enhanced by 15% when dispersed with silica doped silver parti-
Brownian motion induced convection intensifies and the effective TC in- cles. They attributed the enhancements to the presence of fixed dis-
creases. This observation is in agreement with the behavior of ZnO– tances of the Ag NPs on the silica support which allowed for shorter
TiO2/EG [32] and ND-Coe3O4 [33] HyNFs. pathways for the phonon transport amongst dispersed particles. Ac-
Fig. 9 shows the thermal conductivity ratio of the SiC-CuO/C hybrid cording to Nabil et al. [57], the unique nature of the SiO2/TiO2 NC ar-
NFs at different temperatures. It is observed that the TC increases as rangement incentivized the HyNF's greater contact area for
the NC concentration increases. A maximum percentage relative TC en- conduction better than the case of single-particle. These observations
hancement 100∙(knf – kbf /kbf) of 19.3% was observed with the 3.13% wt point to the conclusion that the larger specific surface areas of afforded
concentration of the NF at 333.15 K. The enhancements have been at- by composite particles help strengthen the thermal interactions in the
tributed to the collision of NPs (Brownian motion). There are no data suspension by virtue of the Brownian motion and particle aggregation
available for SiC-CuO/C to directly compare with our results. Neverthe- mechanisms [64]. Hence, SiC-CuO/C HyNF was found to have signifi-
less, the observations revealed that the degree of TC enhancement ob- cantly higher TC enhancement values than the single-component SiC
tained was comparable with those reported with other HyNFs at NF. This superior TC of HyNFs agrees with results in the literature
similar particle loadings. Akilu et al. [31] prepared a TiO2−CuO/C NC [21,40].
Several theoretical models have been proposed for predicting the TC
of suspensions based on the TC of the particles, base fluid, volume
Fig. 8. Photograph of different samples of SiC-CuO/C–EG hybrid nanofluids stored at room Fig. 9. Relative thermal conductivity of SiC-CuO/C hybrid nanofluids at different
temperature of 298.15 K for 30 days. temperatures.
S. Akilu et al. / Powder Technology 354 (2019) 540–551 547
Table 5
Fitting parameters A, B, and deviation AAD%, of linear model from thermal conductivity
data of SiC-CuO/C nanofluid.
φm/wt%
are presented in Table 5. The small value of the relative model error
for the thermal conductivity suggests good consistency with the
experimental data.
In order to describe the TC behavior for the base liquid and NF com-
bined, regression analysis has been performed with the experimental
Fig. 10. Comparison of relative thermal conductivity enhancements of single-particle SiC data for calculating the TC of the SiC-CuO/C hybrid NF as a function of
and SiC-CuO/C nanocomposite hybrid nanofluids.
the particle volume concentration and temperature as follows:
12:5543
concentration, and particle shape. The effective medium approach of the knf T
kr ¼ ¼ 1:0426 þ 0:5003½φv 0:8153 ð5Þ
Maxwell [65] and Hamilton-Crosser [66] models are: kbf To
Maxwell model
where, the reference temperature To = 273.15 K. This correlation has
knf kp þ 2kbf þ 2φ kbf −kp very high accuracy, with a correlation coefficient R2 (0.9229), valid for
¼ ð2Þ
kbf kp þ 2kbf −φ kbf −kp a temperature range of 298.15 K–333.15 K, and the volume fraction con-
centration range of 0.25–0.99%.
Hamilton-Crosser model The predicted values from the developed correlation (Eq. (5)) were
further compared with the experimental data as presented in Fig. 12.
knf kp þ ðn−1Þkbf −ðn−1Þφ kbf −kp The model was in good agreement with the experimental data, with
¼ ð3Þ
kbf kp þ ðn−1Þkbf þ φ kbf −kp ± 2.0% mean absolute deviation (MAD). The sum of the squared errors
(SSE) and the average absolute deviation (%AAD) for the developed cor-
Hybrid nanofluids are new solid/liquid-mixtures and there is a lack relation was determined to be 0.22% and 0.72%, respectively.
of data available for the TC of NC particles in the literature. Thus, a direct
comparison with the above-mentioned theoretical models is not possi- 3.4. Rheology and viscosity of the SiC-CuO/C nanofluids
ble. Moreover, predictions of these classical correlations do not match
the experimental results due to non-inclusion of thermal interfacial re- Several reports have been presented concerning the application of
sistance in modeling [61]. Data from a recent report revealed up to a 6% rheometers to analyze the rheology of NFs [28,56,68]. Comprehensive
deviation of the experimental data from the model prediction [67]. On rheological characterization undertaken by the authors confirms that
the other hand, the thermal conductivity of EG-based NFs can be the NFs can exhibit either or both Newtonian and Non-Newtonian be-
modeled closely by a linear function as presented in the literature havior depending on factors such as the particle size, concentration,
[18]. In a similar way, the thermal conductivity of the SiC-CuO/C HyNF and base liquid viscosity. The NFs assume the Newtonian behavior
is represented with the function of temperature according to the ex- when the concentration of the NPs is low for the case of the Al2O3–Cu/
pression as follows: water hybrid [56]. The Newtonian behavior of the fluids is represented
according to the governing equation which is given by:
knf ðT Þ ¼ A þ BT ð4Þ
τ ¼ ηγ_ ð6Þ
where, A and B are the fitting parameters. Fig. 11 show that the profiles
fitted to the linear equation and it is observed that the TC data fitted the where τ is the shear stress, η is the coefficient of viscosity, and γ_ is the
linear model well at different temperatures. The fitting parameters (A, shear rate. To investigate the rheological characteristics of the HyNFs,
B) and the deviation between the fitted data and the measurements
Fig. 11. Measured thermal conductivities of SiC-CuO/C hybrid nanofluids as a function of Fig. 12. Parity plot for thermal conductivity ratio data points for SiC-CuO/C–EG hybrid
temperature. nanofluids.
548 S. Akilu et al. / Powder Technology 354 (2019) 540–551
Table 6
Dependence of viscosity on particle concentration and temperature on thermal conductivity of SiC-CuO/C nanofluid.
φm/wt% ηbf/Pa·s
298.15 K 303.15 K 308.15 K 313.15 K 318.15 K 323.15 K 328.15 K 333.15 K 338.15 K 343.15 K 348.15 K 353.15 K
0.00 0.0163 0.0134 0.0111 0.0092 0.0076 0.0066 0.0057 0.0048 0.0042 0.0035 0.0032 0.0029
0.82 0.0204 0.0173 0.0144 0.0115 0.0102 0.0089 0.0079 0.0062 0.0055 0.0045 0.0040 0.0038
1.62 0.0233 0.0193 0.0167 0.0135 0.0118 0.0104 0.0089 0.0078 0.0069 0.0056 0.0050 0.0045
2.42 0.0276 0.0223 0.0197 0.0159 0.0138 0.0122 0.0106 0.0090 0.0079 0.0061 0.0057 0.0052
3.13 0.0335 0.0264 0.0223 0.0186 0.0156 0.0134 0.0115 0.0102 0.0088 0.0075 0.0067 0.0060
Table 7
Fitting parameters ηo, A, B, and deviation AAD%, of Vogel–Fulcher–Tammann equation
from dynamic viscosity data of SiC-CuO/C hybrid nanofluids.
φm/wt%
ηnf where, T is the temperature in K, ln ηo, A, and B are the fitting parame-
¼ 1 þ 2:5φ ð7Þ
ηbf ters. To ascertain the goodness of VFT fitting, the experimental data of
the viscosity is shown along with the predicted values from Eq. (9) in
Fig. 16. The values of the VFT parameters and deviation of the model
de-Bruijn model
predictions are listed in Table 7. The VFT model has been effectively
ηnf used by the authors to correlate the temperature dependence of the vis-
¼ 1 þ 2:5φ þ 4:698φ2 ð8Þ cosity of EG-based NFs, for example, Żyła et al. [75] for BN/EG and
ηbf
Pastoriza-Gallego et al. [68,76] respectively for Al2O3-EG and ZnO/
EG NFs.
For representation of the NF viscosity in terms of volume fraction of
NC particles and temperature, a linear multiple regression analysis was
undertaken, leading to a new viscosity correlation as follows:
0:8544
ηnf T
ηr ¼ ¼ 1:0855 þ 18:9440½φv 1:0757 6:2096 ð10Þ
ηbf To
Fig. 16. Measured viscosities of SiC-CuO/C hybrid nanofluids as a function of temperature. Fig. 17. Parity plot for viscosity ratio data points for SiC-CuO/C–EG hybrid nanofluids.
550 S. Akilu et al. / Powder Technology 354 (2019) 540–551
Nomenclature
cη viscosity enhancement coefficient [−]
ck thermal conductivity enhancement coefficient [−]
cr heat transfer enhancement ratio [−], cr = cμ/ck
d diameter [nm]
k thermal conductivity [W m−1 K−1]
kr thermal conductivity ratio [−], knf/kbf
kr, nf thermal conductivity enhancement [%], kr, nf = 100(knf − kbf)/
kbf
n empirical shape factor [−]
t time [s]
T temperature [K]
To reference temperature
Fig. 18. Plot of predicted laminar heat transfer enhancement ratio vs. nanoparticle mass Greek symbols
concentrations. η dynamic viscosity [mPa∙s]
ηr viscosity ratio [−], ηnf/ηbf
ηr, nf viscosity enhancement [%], ηr, nf = 100(ηnf − ηbf)/ηbf
3.5. Figure of the merit/property enhancement ratio γ_ shear rate [s−1]
φ particle concentration [%]
The heat transfer performance of NFs under a fully developed lami- τ shear stress [dyne cm−2]
nar flow in a tube could be predicted based on the viscosity and TC en-
hancements of the NFs as suggested by Prasher [77]. The investigators Subscripts
concluded that the increase in viscosity has to be more than four bf base fluid
times larger than the increase in the TC for the NF not to be beneficial exp experiment
thermal fluids according to the following expression: m mass
nf nanofluid
p particle
cη ηr −1 pred prediction
¼ ≤4 ð11Þ
ck ðkr −1Þ s shape
v volume
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