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31 (
3
); 412-426
doi:
10.1016/j.jksus.2017.09.016

Predicting the effective viscosity of nanofluids based on the rheology of suspensions of solid particles

Department of Chemical and Process Engineering, University of Moratuwa, Sri Lanka

⁎Corresponding author at: University of Moratuwa, Moratuwa, Sri Lanka. iamdilansanjaya@gmail.com (Dilan S. Udawattha),

Disclaimer:
This article was originally published by Elsevier and was migrated to Scientific Scholar after the change of Publisher.

Peer review under responsibility of King Saud University.

Abstract

Abstract

The development of nanofluid as an innovative class of thermal fluid subsequently inspired use in their engineering applications. As a result, the necessity of experimental work to determine the thermophysical properties of nanofluids affecting heat transfer such as specific heat capacity, viscosity, thermal conductivity and density. Theoretical models are used in numerical studies of engineering applications to calculate thermophysical properties. This study intends to develop a new correlation for calculating the effective viscosity of nanofluids. In the model, we considered an effect of interfacial layer on the nanoparticle, the interfacial layer on nanoparticle works as a solid like layer in between the base fluid and nanoparticle surface. When nanoparticles are suspended in the base fluid, Brownian motion occurs due to the relative velocity of the base fluid and nanoparticles, which is also incorporated in this model. The correlation developed successfully express in outcome advance the viscosity of a variety of nanofluids, (Al2O3, Fe, hexagonal boron nitride (hBN), ZnO)-Ethylene Glycol, (Al2O3, hBN, SiC)-Ethylene Glycol Water mixture, (CuO, Al2O3, Fe3O4, TiO2, hBN, Graphite, Single-wall carbon nanotube (SWCNT))-water, (Fe3O4)-Toluene. The new correlation was derived from 501 viscosity values of nanofluid, 75% of them are within the correlation coefficient 0.78–1 and mean deviation less than 5%.

Nomenclature

h s

inter particle spacing (m)

d p

diameter of a particle (m)

r

radius of a nanoparticle (m)

h

thickness of a nanolayer (m)

V B

Brownian velocity

T

temperature

N A

Avogadro constant

r p

radius of a particle

r r

relative radius

M p

mass of a particle

A p

area of a particle

C f

correction factor

c

constant

Z

linear equation 1

A

factor

B

linear equation 2

k B

Boltzmann constant

Greek symbols

μ nf

dynamic viscosity of nano fluid

μ bf

μ enf

ρ p

particle density (kg m3)

ρ l

liquid density (kg m3)

m ·

maximum particle volume (m3)

μ ST

static part of viscosity of nanofluid

μ DY

dynamic part of effective viscosity of nanofluids

μ BM

viscosity due to Brownian motion

ϕ m

mass fraction

ϕ e

effective volume fraction

volume fraction

δ

distance between the nanoparticles (m)

ρ

density (kgm3)

μ enf

experimental dynamic viscosity of nanofluid

α n , β n , γ n

functions

Subscripts

nf

nano fluid

bf

base fluid

p

particle

l

liquid

Abbreviation

EG

Ethylene glycol

BM

Brownian motion

Re

Reynolds number

EM

Einstein model

DY

dynamic

ST

static

1

1 Introduction

Nanofluid is a novel class of fluid, which is developed by dispersing nano-sized particles in base fluid (Kasaeian et al., 2015; Nkurikiyimfura et al., 2013; Angayarkanni and Philip, 2015; Raja et al., 2016). The heat transfer and fluid flow processes consist of active roles in chemical processors, automotive, air conditioning and power generation (Mar et al., 2015; Zhai et al., 2015; Sheremet et al., 2015; Ghanbarpour et al., 2015; Mahian et al., 2013; Alawi and Sidik, 2015). Base fluids such as engine oil, ethylene glycol or water were extensively used as heat transferring fluids in many industries (Esfe et al., 2015). Stephan U.S. Choi invented that high thermal conductivity nanofluid, such as engine oil, water or ethylene glycol, can be formed by dispersing nanosize particles into some conventional heat transfer fluids (Choi and Eastman, 1995).

There are four theoretical models related to fluid namely viscosity, thermal conductivity, density and specific heat capacity. The viscosity and rheological properties of nanofluids are also crucial for their thermal and energy applications. In fact, pumping power in energy and heat systems is related to nanofluids viscosity, and pressure drop in flow systems is directly linked to viscosity. Moreover, viscosity influences heat transfer enhancement of nanofluids from forced convection and natural convection and appear in many dimensionless numbers and coefficients such as Prandtl number, Brinkman number, Reynolds number, Rayleigh number, and Colburn j factor used in thermal and fluids sciences (Murshed and Estellé, 2017).

The most important thermo-physical property of nanofluid is viscosity, which is mainly affected by convective heat transfer and the pumping power requirement. It is evident that convective heat transfer coefficient increases with an increment of nanoparticle volume fraction. Moreover, the pumping power requirement reduces with nanoparticle loading. Hence precise figures on the effective viscosity of nanofluids are critical for industrial applications of nanofluids (Yang et al., 2012).

Einstein (1906), Brinkman (1952) and Batchelor (1977) developed analytical models to estimate viscosity values of composites and mixtures at the beginning of the twentieth century. Those analytical models were failed dramatically predicting viscosity of nanofluid, which are based on a well-established theory of colloid including particles of the order of micrometer or millimeter. Thus new models based on the viscosity of nanofluid have been proposed. They mainly considered interfacial layer on the nanoparticle (Avsec and Oblak, 2007). One of them based on Brownian motion of nanoparticle in the base fluid (Masoumi et al., 2009).

It has been proven beyond doubt that the liquid molecules are arranged themselves into an ordered layer at the solid-liquid interface (Yu et al., 2000), so that the thermal conductivity in that ordered layer is smaller than a thermal conductivity of the solid particles but larger than that of the base fluid. This interfacial layer is a solid-like structure, and it is referred to as nanolayer. This hypothetical nanometre size layer is considered as a thermal layer between the solid particle surface and the base fluid. Nanolayer is one of the likely mechanisms behind thermal conductivity enhancement and has been proposed by many research groups (Leong et al., 2006; Wang et al., 2003; Yu and Choi, 2003; Murshed et al., 2009). Yu and Choi suggested a renovated Maxwell correlation, which was considered the effect of the nanolayer. They have demonstrated that existence of even a thin nanolayer could considerably boost the thermal conductivity of nanofluids, mainly when the particle diameter is smaller than 10 nm (Yu and Choi, 2003). Tso et al. proposed an exponential decay equation for the nanolayer thickness and the nanoparticle radius for different types of nanofluids (Tso et al., 2014).

It can be argued that the reason for extra energy transport of nanoparticles is due to result of Brownian motion. The relative motion between nanoparticles and base fluid molecules generates micro-convection (Shukla et al., 2016). Jang and Choi proposed an initial model based on the convection, which affects by Brownian motion of the particles (Jang and Choi, 2004). However, Ravi Prasher showed that the correlation proposed by Jang and Choi is incorrect and he developed a new correlation for effective thermal conductivity of nanofluid based on Brownian motion (Prasher et al., 2006; Prasher et al., 2005). Masoumi et al. have presented improved correlation for viscosity of nanofluid with the foundation of Ravi Prasher correlation for thermal conductivity of nanofluid (Masoumi et al., 2009). Koo and Kleinstreuer proposed a correlation for the viscosity of nanofluid employing the same concept to develop thermal conductivity of nanofluid, which is based on Brownian motion of nanoparticle (Koo and Kleinstreuer, 2005). Keblinski et al. contended that the motion as a result of Brownian motion is negligible (Phillpot and Eastman, 2016).

Yang et al. found the temperature impact over the viscosity of nanofluid. They have used graphene as the nanomaterial in experiments. They showed that the viscosity declines with the increase of temperature (Yang et al., 2005). Chen et al. studied the same effect of MWCNT-distilled water nanofluid for 278 K–338 K and showed that viscosity ratio increases expressively with temperature after 338 K (Chen et al., 2008).

He et al. showed that experimental values of nanofluid viscosity increase with intense the size of the particle (He et al., 2007). However, Lu and Fan discovered that viscosity of nanofluid declines with increases of a radius of the particle (Lu and Fan, 2008). Chevalier et al. investigated the experimental viscosity values of SiO2-Ethanol nanofluid for different particle radius such as 17, 47, 95 nm and revealed that viscosity rises with the decreasing the diameter of the particle (Chevalier et al., 2007). Prasher et al. found that nanofluid viscosity is not depending on nanoparticle diameter (Prasher et al., 2006).

Chevalier et al. experimentally found that viscosity abnormally increases when an increase in volume concentrations (Chevalier et al., 2007). Lu and Fan discovered that experimental viscosity values of nanofluids evolve into advanced as the volume fraction rises (Lu and Fan, 2008). Chen et al. found that viscosity increases after a 0.4% of volume fraction (Chen et al., 2008). Phuoc and Massoudi discovered Fe2O3-deionized water nanofluids experimental viscosity values rises with increasing particle volume concentration (Phuoc and Massoudi, 2009). Nguyen et al. found in their study of Al2O3-water 530 percentage increment in viscosity when volume fraction increases from 0 to 12% (Nguyen et al., 2008).

Garg et al. discovered a fourfold advancement in experimentally viscosity values when compare the Einstein model (Garg et al., 2008). Mahbubul et al. cited as no correlation can forecast the experimental viscosity values exactly in a broad range of particle volume concentration (Mahbubul et al., 2012). Murshed et al. discussed that the well-established models such as Einstein (1906), Krieger and Dougherty (1959) and Batchelor (1977) could not forecast the experimental viscosity values in an exact way (Murshed et al., 2008).

In previous studies, many models were developed to evaluate effective viscosity of nanofluids by considering Brownian motion. The aim of the present work is to develop a new correlation for the effective viscosity of nanofluids while considering the interfacial layer on nanoparticle and Brownian motion. The current model compared with the classical model of Einstein (1906) and predictions of Wang et al. (1999) with the selected experimental results of nanofluids as a function of the parameters such as a material of nanoparticle, nanoparticle size, volume fraction, and temperature.

2

2 Theoretical models

Presently, various theoretical correlations have been introduced to model the dependence of nanofluid viscosity with the fluid characteristics.

2.1

2.1 Einstein model

Einstein derived the applicable first theoretical formula for the estimation of viscosity values of composites or mixtures in 1906. This model developed while assuming linear viscous fluid including suspensions of rigid and spherical particles. Einstein’s model is valid for very low volume fraction (∅ < 0.02) Einstein, 1906.

(1)
μ EM nf = μ bf ( 1 + 2.5 )
(2)
ϕ = ρ l ϕ m ρ l ϕ m + ρ p ( 1 - ϕ m )

2.2

2.2 Brinkman model

Brinkman modified Einstein’s model for used with average particle volume fraction up to 4% (Brinkman, 1952).

(3)
μ nf = μ bf 1 ( 1 - ) 2.5

2.3

2.3 Batchelor model

Batchelor reformed Einstein’s theoretical model by presenting Brownian motion effect (Batchelor, 1977).

(4)
μ nf = μ bf ( 1 + 2.5 + 6.5 2 )

2.4

2.4 Graham model

Graham has proposed a generalization of Batchelor model. His formula is agreed well with Einstein’s model for volume fraction lower than 0.02. Graham’s model is as follows (Mori and Ototake, 1956).

(5)
μ nf = μ bf 1 + 2.5 + 4.5 1 h s d p 2 + h s d p 1 + h s d p 2

2.5

2.5 Wang et al. model

Wang et al. found a model to predict viscosity of nanofluid as follows (Wang et al., 1999).

(6)
μ nf = μ bf ( 1 + 7.3 + 123 2 )

2.6

2.6 Avsec and Oblak model

Avsec and Oblak cited as renewed Ward model as follows (Avsec and Oblak, 2007).

(7)
μ nf = μ bf ( 1 + 2.5 ϕ e + ( 2.5 ϕ e ) 2 + )
(8)
ϕ e = ϕ 1 + h r 3
(9)
μ nf = μ bf 1 1 - 2.5 ϕ e

2.7

2.7 Masoumi et al. model

Masoumi et al. suggested a new viscosity correlation by considering Brownian motion of nanoparticle in nanofluid (Masoumi et al., 2009).

(10)
μ nf = μ bf 1 + ρ p × V B × d p 2 72 × δ × C
(11)
V B = 18 × R × T π × N A × ρ p × d p 3
(12)
δ = π × d p 3 6 × 3
(13)
C = { ( - 1.133 × d p - 2.771 ) + ( 0.09 × d p - 0.393 ) } × 10 - 6

3

3 Methodology

3.1

3.1 Experimental database

The primary goal of the current work is to present an advance model, which is capable of predicting the effective viscosity for different size of nanofluids. The current model was developed based on an extensive range of experimental values of nanofluid viscosity, which were acquired from following literature (Table 1). Various types of base fluids, such as water, ethylene glycol, ethylene glycol-water mixture and toluene containing different types of particles nanomaterial, like Al2O3, Fe, hBN, ZnO, SiC, CuO, Fe3O4, TiO2, Graphite, and SWCNT were used for making this model (Table 2). The experimental database, which is used in this study, is shown in Table 1.

Table 1 Summary of experimental data of viscosity of nanofluids from different researches.
No Base fluid Nano particle type Particle size (nm) Volume fractions (%) Temperatures (K) Reference Data points
1 EG Al2O3 43 0.5,1,1.5,2.1,3.1,4.8,6.6 283.15,288.15,293.15,298.15,303.15,308.15,313.15,323.15 Pastoriza-Gallego et al. (2011a) 56
2 EG Al2O3 8 0.5,1,1.5,2.1,3.1 283.15,288.15,293.15,298.15,303.15,308.15,313.15,323.15 Pastoriza-Gallego et al. (2011a) 40
3 Water CuO 33 *wt(%)1,1.74,2.5,3.5,5,7,10 283.15,288.15,293.15,298.15,303.15,308.15,313.15,323.15 Pastoriza-Gallego et al. (2011b) 56
4 Water CuO 11 *wt(%)1,2.5,3.5,5,7,10 283.15,288.15,293.15,298.15,303.15,308.15,313.15,323.15 Pastoriza-Gallego et al. (2011b) 48
5 Water Graphite 8 0.5,1,1.5,2 293,303,313,323,333 Dalkilic et al. (2016) 20
6 Water Al2O3 25 0.5,1,2,3,4 283,288,293, *298 (0.5,1,2) Mena et al. (2013) 18
7 EG:Water = 20:80 Al2O3 36 0.3,0.6,0.8,1 293 Syam Sundar et al. (2014) 4
8 Water TiO2 21 0.2,0.6,1,1.5,2 288,298,308 Duangthongsuk and Wongwises (2010) 15
9 EG Fe 40 0.125,0.25,0.5,1 299,308,318,328 Hemmat Esfe et al. (2014) 16
10 EG Fe 70 0.125,0.25,0.5,1 299,308,318,328 Hemmat Esfe et al. (2014) 16
11 EG Fe 100 0.125,0.25,0.5,1 299,308,318,328 Hemmat Esfe et al. (2014) 16
12 Water CNT 9 0.0554,0.277,0.554,1.1,2.8,4.2,5.6 273,283,293,303,313 Halelfadl et al. (2013) 35
13 Water hBN 70 0.5,1,2,3 298 İlhan et al. (2016) 4
14 Water: EG = 50:50 hBN 70 0.5,1,2,3 298 İlhan et al. (2016) 4
15 EG hBN 70 0.5,1,2,3 298 İlhan et al., 2016 4
16 Water TiO2 95 0.25,0.6,1.2 298 He et al. (2007) 3
17 Water SWCNT 45 1.25,2.5,5,7.5 303,308,313,318,323,328,333 Baratpour et al. (2016) 28
18 Toluene Fe3O4 10 0.19,0.31,0.4,0.5 298,308,318,328,338 Singh et al. (2015) 20
19 Water: EG = 60:40 SiC 30 0.2,0.4,0.6,0.8,1 283.15,288.15,293.15,298.15,303.15,308.15 Li and Zou (2016) 30
20 EG ZnO 100 0.5,1,2,3,4 293,308,323,338,353 Lee et al. (2012) 25
21 Water Nano-diamond (ND) 12 0.2,0.4,0.6,0.8,1 293,303,313,323,333 Sundar et al. (2016) 25
22 Water Fe3O4 25 0.1,0.2,0.4,1,2,3 293,298,308 Toghraie et al. (2016) 18
23 Coconut oil CuO 40 *wt(%)0.5,1,1.5,2,2.5 308,318,328 Nabeel Rashin and Hemalatha (2013a) 15
24 Coconut oil ZnO 40 *wt(%)0.5,1,1.5,2,2.5 308,318,328 Nabeel Rashin and Hemalatha (2013b) 15
25 EG AlN 43 *wt(%) 0.05,0.1,0.15,0.2 293.6 Żyła and Fal (2016) 4
Table 2 Summary of nanofluids.
No Type Description Data points
1 Base fluids Water, EG, (Water:EG)-50:50, (Water:EG)-80:20, (Water:EG)-40:60 and Toluene, Coconut oil 7
2 Nanoparticle materials Al2O3, CuO, Graphite, TiO2, Fe, Fe3O4, hBN, SWCNT, SiC, ZnO, AlN 11
3 Nanofluids Based on nanomaterial and base fluid 25
4 Fluids Based on volume fractions 128
5 Experimental data points Based on volume fractions into temperatures 535

3.2

3.2 Factors consider in the new correlation

The Einstein model well predicts viscosity values of the suspension containing particles volume fraction less than 0.02. Therefore Einstein model can be applicable for nanofluid. However, Garg et al. discovered that experimental results higher than viscosity values of nanofluid predicted by the Einstein model (Garg et al., 2008). Moreover, Hemmat Esfe et al. (2014) observed the effective viscosity of nanofluid depends on particle size. That implies the effective viscosity of nanofluid depends on some other factors other than volume fraction. Brownian velocity is introduced due to Brownian motion of nanoparticles within the base fluid. Masoumi et al. (2009) developed a theoretical model for effective viscosity of nanofluid by considering Brownian motion effect.

4

4 Description of the new correlation

4.1

4.1 Development of the model

Brownian motion of nanoparticles was contemplated together with the outcome of fluid particles moving beside nanoparticles situated on sides of them (Koo and Kleinstreuer, 2005). Masoumi et al. developed a model for the viscosity of nanofluids by adding base fluid viscosity and effective viscosity due to Brownian motion (Masoumi et al., 2009).

(14)
μ nf = μ bf 1 + ρ p × V B × d p 2 72 × δ × C
(15)
V B = 18 × R × T π × N A × ρ p × d p 3
(16)
δ = π × d p 3 6 × 3
(17)
C = { ( - 1.133 × d p - 2.771 ) + ( 0.09 × d p - 0.393 ) } × 10 - 6

Brownian motion part of Masoumi et al. model as follows (Masoumi et al., 2009),

(18)
μ BM = ρ p × V B × d p 2 72 × C f × δ

Correction factor ( C f )

(19)
μ BM μ bf = ρ p × V B × d p 2 72 × C f × δ × μ bf
(20)
Z = C f × μ bf
(21)
Z = A - B

When the particle size in micrometer, μ BM = ρ p × V B × d p 2 72 × C f × δ 0

Hence, d p > 1 μ m μ s μ bf ( 1 + 0 ) μ s μ bf

According to the rheology of suspensions of solid particles when the particle size in micrometer viscosity of the suspension is higher than the base fluid. Hence there should be a part related to volume fraction.

Einstein in 1906 has derived the applicable first theoretical formula for the estimation of viscosity values of composites or mixtures (Einstein, 1906).

(22)
μ EM nf = μ bf ( 1 + 2.5 )

Viscosity effect due to nanolayer

(23)
μ NL nf = μ bf ( 2.5 ϕ e ) - μ bf ( 2.5 )
(24)
μ ST = μ EM nf + μ NL nf
This part consider as a static part,
(25)
μ ST = μ bf ( 1 + 2.5 ϕ e )
Finally model as follows,
(26)
μ nf = μ bf 1 + 2.5 ϕ e + ρ p × V B × d p 2 72 × C f × δ

By analyzing several experimental results, an equation for Z obtained as follows.

(27)
Z = T × 10 - 10 × - 0.002 T - 0.284
(28)
C f = μ bf - 1 [ T × 10 - 10 × - 0.002 T - 0.284 ]

The Brownian motion part consider as a dynamic part,

(29)
μ DY = μ bf ρ p V B d p 2 72 δ [ T × 10 - 10 × - 0.002 T - 0.284 ]

4.2

4.2 The new correlation

The effective viscosity is combination of static and dynamic parts of nanofluid viscosity, and then it can be stated as follows,

(30)
Effective Viscosity of nanofluid = Static part of the effective viscosity of nanofluid + Dynamic part of the effective viscosity of nanofluid μ nf = μ ST + μ DY
(31)
μ nf = μ bf 1 + 2.5 ϕ e + ρ p × V B × d p 2 72 × δ × [ T × 10 - 10 × - 0.002 T - 0.284 ]

5

5 Results and discussion

5.1

5.1 Statically analysis

The present model was validated by using experimental data. In the statical evaluation authors used two statistical indicators median deviation (MD) and correlation coefficient (R2). The mean deviation specifies that how much two groups of data are correlated. The correlation coefficient shows that how much closer to one group of data set with another group of data set.

(32)
MD = 1 n 1 n ABS μ ef - μ nf μ ef × 100
(33)
R 2 = 1 - i = 1 n ( μ Enf - μ nf ) 2 i = 1 n ( μ Enf - μ Enf ) 2

The present model suits with the 501 viscosity values with mean deviations lower than 5% and 75% of them are within the correlation coefficient 0.78–1.

5.2

5.2 Present model comparison with existing theoretical models

Existing models Einstein (1906), Brinkman (1952), Batchelor (1977), Wang et al. (1999) and Masoumi et al. (2009), are expressively underpredicted the experimental data (Figs. 1–5). The developed model is in excellent agreement with the experimental data (Table 3). It was found that Masoumi et al. (2009) model predicts viscosity lower than base fluid, which is due to its correction factor. Masoumi et al. model (Masoumi et al., 2009) valid only for the following conditions (Eq. 41).

(34)
< ( 0.09 × d p - 0.393 ) ( 1.133 × d p + 2.771 )
Comparison of the theoretical predictions with the experimental results for Fe3O4-Water, Particle size 25 nm at 20 °C.
Fig. 1
Comparison of the theoretical predictions with the experimental results for Fe3O4-Water, Particle size 25 nm at 20 °C.
Comparison of the theoretical predictions with the experimental results for Carbon Nanotube-Water, Particle size 9 nm at 10 °C.
Fig. 2
Comparison of the theoretical predictions with the experimental results for Carbon Nanotube-Water, Particle size 9 nm at 10 °C.
Comparison of the theoretical predictions with the experimental results for Al2O3-Water, Particle size 36 nm at 20 °C.
Fig. 3
Comparison of the theoretical predictions with the experimental results for Al2O3-Water, Particle size 36 nm at 20 °C.
Comparison of the theoretical predictions with the experimental results for SiC-EG: Water = 40:60, Particle size 30 nm at 10 °C.
Fig. 4
Comparison of the theoretical predictions with the experimental results for SiC-EG: Water = 40:60, Particle size 30 nm at 10 °C.
Comparison of the theoretical predictions with the experimental results for Al2O3-EG, Particle size 43, 8 nm at 10 °C.
Fig. 5
Comparison of the theoretical predictions with the experimental results for Al2O3-EG, Particle size 43, 8 nm at 10 °C.
Table 3 Comparison of the theoretical predictions with the experimental results.
Figure Nanomaterial Base fluid Particle size (nm) MD% R2 Experimental Data
Fig. 1 Fe3O4 Water 25 3.2 0.95 Toghraie et al. (2016)
Fig. 2 CNT Water N/A 1.4 0.83 Halelfadl et al. (2013)
Fig. 3 Al2O3 Water 36 1.7 0.78 Syam Sundar et al. (2014)
Fig. 4 SiC Ethylene Glycol 30 3.8 0.43 Li and Zou (2016)
Fig. 5 Al2O3 Ethylene Glycol 8 2 0.95 Pastoriza-Gallego et al. (2011a)
Fig. 5 Al2O3 Ethylene Glycol 43 1.4 0.99 Pastoriza-Gallego et al. (2011a)

5.3

5.3 Effective parameters on the effective viscosity of nanofluid

5.3.1

5.3.1 Effect of particle size

Al2O3–ethylene glycol (Pastoriza-Gallego et al., 2011a) nanofluids exhibit that the smaller particles improve the viscosity compared with larger particles. Fe-Ethylene glycol (Dalkilic et al., 2016), CuO-water (Pastoriza-Gallego et al., 2011b) show a similar pattern (Fig. 6). The new correlation exhibits viscosity’s declining trend with increasing particle size. Particle size effect associated with both the static part and the dynamic part. Then the effect of particle size on the new correlation as follows,

(35)
μ nf = γ 1 + α 1 1 d p 3 + β 1 1 d p 1 2
Effect of volume fraction on viscosity for (a) Fe-EG, particle size 40, 70,100 nm at 55 °C (b) Al2O3-EG, particle size 43, 8 nm at 10 °C.
Fig. 6
Effect of volume fraction on viscosity for (a) Fe-EG, particle size 40, 70,100 nm at 55 °C (b) Al2O3-EG, particle size 43, 8 nm at 10 °C.

5.3.2

5.3.2 Effect of temperature

Mena et al. experimentally measured temperature effect of Al2O3-Water nanofluid viscosity for a temperature range of 283 K–298 K. They experimentally found that dynamic viscosity declines with the increase of temperature (Pastoriza-Gallego et al., 2011a). Pastoriza-Gallego et al. showed the temperature effect of CuO-water nanofluid for eight temperatures (283.15, 288.15, 293.15, 298.15, 303.15, 308.15, 313.15, and 323.15 K) and indicated that relative viscosity decreases with increase of temperature (Pastoriza-Gallego et al., 2011b) (Fig. 7).

(36)
μ nf = γ 2 + α 2 + β 2 1 T × - AT
Effect of volume fraction on viscosity for (a) Al2O3-water, Particle size 25 and 0.5, 1 and 2% volume fractions (b) CuO-water, Particle size 11 nm and 0.165, 0.417, 0.589% volume fractions.
Fig. 7
Effect of volume fraction on viscosity for (a) Al2O3-water, Particle size 25 and 0.5, 1 and 2% volume fractions (b) CuO-water, Particle size 11 nm and 0.165, 0.417, 0.589% volume fractions.

5.3.3

5.3.3 Effect of volume concentration

Dalkilic et al. (2016) and Pastoriza-Gallego et al. (2011a) found that viscosity of nanofluid increased with rising the particle volume fraction (Fig. 8). The present model complies with viscosity’s increasing trend with increasing volume concentration. Volume concentration effect consists of both static part and dynamic part. The effect of volume concentration on the present model as follows,

(37)
μ nf = γ 3 + α 3 ( ) + β 3 1 A
Effect of volume fraction on viscosity for (a) graphene-water, particle size 8 nm at 60 °C (b) Al2O3-EG, particle size 43 nm at 10 °C.
Fig. 8
Effect of volume fraction on viscosity for (a) graphene-water, particle size 8 nm at 60 °C (b) Al2O3-EG, particle size 43 nm at 10 °C.

It is evident that nanofluid must exhibit base fluid properties at the point of volume fraction is zero. The present model shows viscosity of the base fluid at the point volume fraction is zero. One can obtain the same result for Einstein (1906), Batchelor (1977), Brinkman (1952), Wang et al. (1999), Masoumi et al. (2009), models except for Graham model (Mori and Ototake, 1956).

5.3.4

5.3.4 Effect of nanoparticle material

There is no considerable generic model to evaluate effects of nanoparticle material on nanofluid viscosity. The combination of Mena et al. (2013) and Toghraie et al. (2016) findings come into view that viscosity of nanofluid increases with nanoparticle material density (Fig. 9).

Effect of volume fraction on viscosity for Al2O3-water, Fe3O4-water particle size 25 nm at 25 °C.
Fig. 9
Effect of volume fraction on viscosity for Al2O3-water, Fe3O4-water particle size 25 nm at 25 °C.

The present model exhibits viscosity’s increasing trend with increasing nanomaterial density. Nanomaterial density depends on the only dynamic part. The present model expresses the effect of Nanomaterial density as follows,

(38)
μ nf = γ 4 + α 4 + β 4 ( ρ p )

5.3.5

5.3.5 Effect of particle shape

The Present model developed while assuming nanoparticles are rigid and spherical. Carbon nanotubes are cylindrical with dimensions: radius in nanometer and length in micrometer. As an example, Sundra L.S. et al. cited their research paper Multi-walled carbon nanotubes (MWCNT) outer diameter of 10–30 nm and length of 0.5–500 μm (Sundar et al., 2014) (Fig. 10).

Effect of volume fraction on viscosity for carbon nanotube-water, particle size 9.2 nm at 20 °C.
Fig. 10
Effect of volume fraction on viscosity for carbon nanotube-water, particle size 9.2 nm at 20 °C.

5.4

5.4 Comparison of dynamic and static parts

Numerous authors have suggested semi-empirical models described the relative viscosity of concentrated suspensions, as a function of the volume concentration and compared with the Einstein model (Einstein, 1906). The present model consists of two parts namely the static part and the dynamic part. The static part is a function of volume fractions and ratio of nanolayer thickness to nanoparticle radius. It may be a debatable point to consider, where the dynamic viscosity part is negligible. Fig. 11 shows the experimental viscosity values of Pastoriza-Gallego et al. (2011a) and Pastoriza-Gallego et al. (2011b) (Fig. 11). It can be concluded as the effect of the dynamic part in viscosity ratio increased with increasing the particle concentration. Furthermore, the proportion of dynamic part in viscosity ratio depends on nanoparticle size, nanofluid temperature and density of nanomaterial.

Effect of volume fraction on viscosity for (a) CuO-water, particle size 11 nm at 10 oC (b) Al2O3-EG, particle size 43 nm at 10 °C.
Fig. 11
Effect of volume fraction on viscosity for (a) CuO-water, particle size 11 nm at 10 oC (b) Al2O3-EG, particle size 43 nm at 10 °C.

5.5

5.5 Particle size in micrometer

The nanofluid considers as a fluid, which is dispersing nano-sized particles in the base fluid. Einstein model based on the well-established theory of colloid including particles in size of micrometer or millimeter. Experimental results of Pastoriza-Gallego et al. (2011a) used to compare particle size of micrometer and nanometer (Fig. 12).

Effect of particle size on viscosity for Al2O3-water, volume fraction 3.1% at 10 °C.
Fig. 12
Effect of particle size on viscosity for Al2O3-water, volume fraction 3.1% at 10 °C.

When particle size in micrometer,

The dynamic part ρ p × V B × d p 2 72 × δ × [ T × 10 - 10 × - 0.002 T - 0.284 ] 0

Nanolayer thickness to particle radius ratio h r 0

The static part ( 1 + 2.5 ϕ e ) ( 1 + 2.5 )

That implies, present model turned into the Einstein model for the effective viscosity of nanofluid at particle size higher than 1 micrometer. d p > 1 μ m μ nf = μ bf 1 + 2.5 ϕ e + ρ p × V B × d p 2 72 × δ × [ T × 10 - 10 × - 0.002 T - 0.284 ] μ bf ( 1 + 2.5 )

5.6

5.6 Non-Newtonian nanofluid

The many tunable parameters in nanofluids lead to the wide variations in the properties of nanofluids, such as non-Newtonian rheological properties. Based on experimental results, authors have mentioned that nanofluid exhibits shear-thinning non-Newtonian behavior. To conclude, the present model is not valid for non-Newtonian nanofluid (Table 4).

(39)
μ nf = μ bf 1 + 2.5 ϕ e + ρ p × V B × d p 2 72 × δ × [ Z r ]
Table 4 Comparison of Shear rate vs Z equation.
Experimental data Nanomaterial Basefluid Particle size (nm) Shear rate Z equation
Żyła and Fal (2016) AlN Ethylene Glycol 20 5.94 T × 10 - 10 × - 0.002 T - 0.284
14.56 T × 10 - 10 × - 0.002 T - 0.385
244.2 T × 10 - 10 × - 0.002 T - 0.63
494.2 T × 10 - 10 × - 0.002 T - 0.68
790.6 T × 10 - 10 × - 0.002 T - 0.71
1000 T × 10 - 10 × - 0.002 T - 0.73
Nabeel Rashin and Hemalatha (2013a) CuO Coconut oil 20 14.28 T × 10 - 10 × - 0.002 T - 0.04
Nabeel Rashin and Hemalatha (2013b) ZnO Coconut oil 20 14.28 T × 10 - 10 × - 0.002 T - 0.001

The Z equations for Aluminum Nitride-Ethylene glycol, CuO-Coconut oil, and ZnO-Coconut oil same shear rate (14 s−1) are different from each other. Finally, more experimental results in non-Newtonian nanofluid are needed for build a relationship between shear rate and correction factor.

5.7

5.7 Viscosity and nanofluid stability

Surfactants and dispersants are mostly applied to nanofluid as a stabilizer. The addition of surfactants take down the surface tension of host fluids and adds the immersion of particle. Surfactants are normally used to stabilize the nanofluid (Mukherjee and Paria, 2013). Colangelo et al. discovered surfactants effect for nanofluid viscosity (Colangelo et al., 2016). Even though the present model is developed based on assumption nanoparticles are well immersed, it uses experimental data with unstable nanofluids to derive correction factor.

5.8

5.8 Hybrid nanofluids

Researchers and engineers have carried out experiments for hybrid nanofluids, which are immersed nanoparticles consists of two or more dissimilar materials in the base fluid (Botha et al., 2011; Munkhbayar et al., 2013; Nine et al., 2013; Chen et al., 2014). This study suggested a model that determine the viscosity of hybrid nanofluids are as follows. Furthermore, this model can be expanded for three or four materials. Researchers could perform experimental studies for the viscosity of hybrid nanofluid and develop a general empirical equation.

(40)
μ hnf = μ bf 1 + 2.5 ϕ e 1 + ρ p 1 × V B 1 × d p 1 2 72 × δ 1 × [ T × 10 - 10 × 1 - 0.002 T - 0.284 ] + 2.5 ϕ e 2 + ρ p 2 × V B 2 × d p 2 2 72 × δ 2 × [ T × 10 - 10 × 2 - 0.002 T - 0.284 ]

6

6 Future works

The present correlation is derived from a wide range of experimental data of the effective viscosity of nanofluids. In most of the experimental studies reported in the literature, just the effects of two or three relevant parameters have been investigated. Therefore, for future works, the researchers would perform experimental studies by considering all of the important factors including temperature, nanoparticle size, nanoparticle material, non-Newtonian nanofluid, type of base fluid, which would lead to generating more accurate correlations to predict the effective viscosity of nanofluid.

7

7 Conclusions

A novel analytical model to determine the effective viscosity of fluid containing homogeneously dispersed rigid and spherical nanoparticles was presented. The effective viscosity of nanofluids is consists of two parts namely static and dynamic. The static part of the viscosity of nanofluid is a combination of Einstein model and viscosity effect due to nanolayer. Viscosity effect due to nanolayer was developed as one nanolayer is around a nanoparticle and its thickness is 1 nm. The dynamic part consists of viscosity effect due to Brownian motion of nanoparticles. Viscosity effect due to Brownian motion was included correction factor. Power function was used to derive correction factor. It depends on temperature and volume fraction. Using numerous experimental results correction factor was developed.

The new correlation was tested with 22 different nanofluids. It was used 501 experimental viscosity values to test the new model, and 75% of them are within the correlation coefficient 0.78–1. The new correlation performed well with experimental results when they are under variations of base fluid, nanoparticle size, volume fraction, temperature, and nanomaterial. It was found the new correlation isn’t valid for non-Newtonian nanofluid. The model has been tested with numerous experimental results containing one type of nanomaterial. It is evident that the present model isn’t valid for hybrid nanofluids. One model has been proposed to predict to the effective viscosity of hybrid nanofluid.

Acknowledgment

The authors would like to express their sincere gratitude for the University of Moratuwa.

Conflict of interest

None declared.

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