Optimization of ultrasonication period for better dispersion and stability of TiO2–water nanofluid

Nanofluids are promising in many fields, including engineering and medicine. Stability deterioration may be a critical constraint for potential applications of nanofluids. Proper ultrasonication can improve the stability, and possibility of the safe use of nanofluids in different applications. In this study, stability properties of TiO₂–H₂O nanofluid for varying ultrasonication durations were tested. The nanofluids were prepared through two-step method; and electron microscopies, with particle size distribution and zeta potential analyses were conducted for the evaluation of their stability. Results showed the positive impact of ultrasonication on nanofluid dispersion properties up to some extent. Ultrasonication longer than 150 min resulted in re-agglomeration of nanoparticles. Therefore, ultrasonication for 150 min was the optimum period yielding highest stability. A regression analysis was also done in order to relate the average cluster size and ultrasonication time to zeta potential. It can be concluded that performing analytical imaging and colloidal property evaluation during and after the sample preparation leads to reliable insights.     

Comparative study on thermal performance of helical screw tape inserts in laminar flow using Al2O3/water and CuO/water nanofluids

This paper presents a comparison of thermal performance of helical screw tape inserts in laminar flow of Al₂O₃/water and CuO/water nanofluids through a straight circular duct with constant heat flux boundary condition. The helical screw tape inserts with twist ratios Y = 1.78, 2.44 and 3 were used in the experimental study using 0.1% volume concentration Al₂O₃/water and CuO/water nanofluids. Nanofluids with required volume concentration of 0.1% were prepared by dispersing specified amounts of Al₂O₃ and CuO nanoparticles in deionised water. The performance analysis of helical screw tape inserts in laminar flow of Al₂O₃/water and CuO/water nanofluids is done by evaluating thermal performance factor for constant pumping power condition. Thermal performance factor of helical screw tape inserts using CuO/water nanofluid is found to be higher when compared with the corresponding value using Al₂O₃/water. Therefore, the helical screw tape inserts show better thermal performance when used with CuO/water nanofluid than with Al₂O₃/water nanofluid.     

Ultrasonically tuned surface tension and nano-film formation of aqueous ZnO nanofluids

Nanofluids’ thermophysical properties and heat transfer performance has been investigated for many years, while research on their surface tension (ST) and wetting behavior is very limited. To assess nanofluids potential as industrial products, a complete picture is required to prove their performance in a specific application. Boiling heat transfer, microfluidics and drug development are among the applications where ST is a variable. ST of water-based ZnO nanofluids were measured in the presence and absence of direct ultrasonication. The experiments covered variation of ST with ZnO concentration (0.05–0.4 vol%), ultrasonication amplitude (40% and 100%) and duration. To the best of the authors’ knowledge, this is the first report of ST– ultrasonication process relation for a nanofluid. Results showed that after direct ultrasonication, nanofluids ST is strongly affected by the temperature raise, and in those cases relative ST may provide a clearer picture. A nano-film over individual and agglomerated nanoparticles spotted via TEM imaging was affected from the ultrasonication. Such a nano-film can play a key role in the anomalous thermal transport and wettability of nanofluids. Statistical analyses revealed that changes in ultrasonication amplitude resulted in a statistically significance difference on nanofluid ST and relative ST. Changes in nanoparticle concentration caused a significant difference on the nanofluid ST while the difference in relative ST was insignificant. Variation of ultrasonication duration caused significant variations on the relative ST while the difference in nanofluid ST was not significant. This work highlights that based on specific applications ST and other related features of any nanofluid can be adjusted employing proper ultrasonication conditions.     

High accuracy photopyroelectric investigation of dynamic thermal parameters of Fe3O4 and CoFe2O4 magnetic nanofluids

The suitability of the photopyroelectric (PPE) calorimetry in measuring the thermal parameters of nanofluids was demonstrated. The main advantages of the method (concerning nanofluids) as compared to classical calorimetric techniques are: high sensitivity and small amount of sample required. The thermal diffusivity and effusivity of some nanofluids based on Fe₃O₄ and CoFe₂O₄ type of nanoparticles (mean diameter 6.5 nm) were investigated by using two PPE detection configurations (back and front). In both cases, the information is contained in the phase of the PPE signal. Due to the high accuracy of the results (within ±0.5%) thermal diffusivity was found to be particularly sensitive to changes in relevant parameters of the nanofluid as carrier liquid, type and concentration of nanoparticles.     

Heat transfer enhancement by application of nano-powder

In this investigation, laminar flow heat transfer enhancement in circular tube utilizing different nanofluids including Al₂O₃ (20 nm), CuO (50 nm), and Cu (25 nm) nanoparticles in water was studied. Constant wall temperature was used as thermal boundary condition. The results indicate enhancement of heat transfer with increasing nanoparticle concentrations, but an optimum concentration for each nanofluid suspension can be found. Based on the experimental results, metallic nanoparticles show better enhancement of heat transfer coefficient in comparison with oxide particles. The promotions of heat transfer due to utilizing nanoparticles are higher than the theoretical correlation prediction.     

The effects of ultrasonication power and time on the dispersion stability of few-layer graphene nanofluids under the constant ultrasonic energy consumption condition

Few-layer graphene (FLG) nanofluids have received widespread interest in recent years due to their excellent thermal and optical properties. However, the low dispersion stability is one of the main bottlenecks for their commercialization. Ultrasonication is an effective method and almost an essential step to improve the stability of nanofluids. This work aimed to determine the optimal ultrasonication process for preparing stable FLG nanofluids, particularly under the constant ultrasonic energy consumption condition. For this purpose, FLG nanofluids were prepared under various amplitudes (20%–80%) and times (33.75–135 min) and evaluated by both sedimentation and optical spectrum analysis techniques. It was found that ultrasonication treatment at 30% amplitude for 90 min was sufficient for proper dispersion of FLG, and a further increase in the ultrasonication power would not benefit the stability enhancement much. However, for FLG nanofluids prepared at amplitudes higher than 30% under the constant ultrasonic energy consumption condition, their stability deteriorated seriously due to the reduced ultrasonication time, while for FLG nanofluids prepared at 20% amplitude for 135 min, they showed the higher stability, which indicates that the stability of FLG nanofluids is more sensitive to ultrasonication time than power. Therefore, a relatively longer ultrasonication time rather than a higher amplitude is recommended to prepare stable FLG nanofluids for practical applications at given ultrasonic energy consumption.     

Fabrication, characterization and measurement of thermal conductivity of Fe3O4 nanofluids

Magnetite Fe₃O₄ nanoparticles were synthesized by a co-precipitation method at different pH values. The products were characterized by X-ray diffraction, Fourier transform infrared spectroscopy, and transmission electronic microscopy. Their magnetic properties were evaluated on a vibrating sample magnetometer. The results show that the shape of the particles is cubic and they are superparamagnetic at room temperature. Magnetic nanofluids were prepared by dispersing the Fe₃O₄ nanoparticles in water as a base fluid in the presence of tetramethyl ammonium hydroxide as a dispersant. The thermal conductivity of the nanofluids was measured as a function of volume fraction and temperature. The results show that the thermal conductivity ratio of the nanofluids increases with increase in temperature and volume fraction. The highest enhancement of thermal conductivity was 11.5% in the nanofluid of 3 vol% of nanoparticles at 40 °C. The experimental results were also compared with the theoretical models.     

Investigation on characteristics of thermal conductivity enhancement of nanofluids

It has been shown that a nanofluid consisting of nanoparticles dispersed in base fluid has much higher effective thermal conductivity than pure fluid. In this study, four kinds of nanofluids such as multiwalled carbon nanotube (MWCNT) in water, CuO in water, SiO₂ in water, and CuO in ethylene glycol, are produced. Their thermal conductivities are measured by a transient hot-wire method. The thermal conductivity enhancement of water-based MWCNT nanofluid is increased up to 11.3% at a volume fraction of 0.01. The measured thermal conductivities of MWCNT nanofluids are higher than those calculated with Hamilton–Crosser model due to neglecting solid–liquid interaction at the interface. The results show that the thermal conductivity enhancement of nanofluids depends on the thermal conductivities of both particles and the base fluid.     

Modeling of nanoparticles’ aggregation and sedimentation in nanofluid

The aggregation and sedimentation of nanoparticles in nanofluid have significant influences on the stability and applicability of nanofluids. The objective of this study is to propose a model to predict the nanoparticles’ aggregation and sedimentation characteristics. The characteristics are evaluated by the concentration of nanoparticles in nanofluid at different time. The concentration of nanoparticles can be calculated according to the speed and location of each nanoparticle. Then, the speed and location of each nanoparticle can be yielded when the forces on each nanoparticle are determined. For the forces on nanoparticles are related to the space structure of nanoparticle clusters, the clusters’ space structures are simulated. Case study shows that the mean deviation of predicted nanoparticle concentration from experimental data for Fullerence + H₂O, Fullerence + Oil and CuO + Oil nanofluids are 25%, 16% and 13%, respectively. The model can provide quantitative prediction of the aggregation and sedimentation characteristics of nanoparticles in nanofluid.     

Experimental comparison of Triton X-100 and sodium dodecyl benzene sulfonate surfactants on thermal performance of TiO2–deionized water nanofluid in a thermosiphon

This study investigates how TiO₂/deionized water nanofluids affect the thermal performance of a two-phase closed thermosiphon (TPCT) at various states of operation, according to the surfactant types. A straight copper tube with an inner diameter of 13 mm, outer diameter of 15 mm, and length of 1 m was used as the TPCT, i.e., heat pipe. The nanofluid utilizing in experiments was prepared by mixing the TiO₂ nano-particles at the rate of 1.3% and a surfactant at the rate of 0.5% with deionized water. The surfactants used for lowering the surface tension give rise to prevent the flocculation in nanofluids. In order to see the influences of the surfactants on the nanofluid properties, two types surfactants, Triton X-100 and sodium dodecyl benzene sulfonate (SDBS), were selected as nonionic and ionic surfactants and used in this study. The nanofluid was charged with in the ratio of 33.3% (equals to 44.2 ml) of the volume of the TPCT. To be able to make experimental comparisons, three different working fluids prepared under the same conditions in the same heat pipe were tested at three different heating powers (200, 300, and 400W) and three different coolant water flow rates (5, 7.5, and 10 g/s). The experiments were conducted for both TiO₂ and Triton X 100–deionized water nanofluid and TiO₂ and SDBS–deionized water nanofluid. The findings obtained from the tests were also compared to each other for showing off to what extent a surfactant affects the nanofluid properties. The maximum improvement in the thermal resistance was achieved by 43.26% in the experiment realized at 200 W input power and 7.5 g/s cooling water mass flow rate, in which the working fluid is TiO₂ and SDBS–deionized water nanofluid.     

Utilization of Fly Ash Nanofluids in Two-phase Closed Thermosyphon for Enhancing Heat Transfer

This study investigates how fly ash nanofluids affect the thermal performance of a two-phase closed thermosyphon at various states of operation. The utilization of nanofluids obtained from X₂O₃-type oxides, such as Al₂O₃, Fe₂O₃, or CuO, on the improvement of two-phase closed thermosyphon performance was reported in a number of studies in the literature. The present study experimentally demonstrated the effect of using a nanofluid obtained from fly ash comprised of various types of metal oxides in varying ratios on improving the performance of a two-phase closed thermosyphon. The fly ash was obtained from the flue gas that was captured in the cyclones of the Yatagan thermal power plant (Turkey). Triton X-100 (Dow Chemical Company) dispersant was used in the study to produce the 0.2% (wt) fly ash/water nanofluid via direct synthesis. A straight copper tube with an inner diameter of 13 mm, outer diameter of 15 mm, and length of 1 m was used as the two-phase closed thermosyphon. The nanofluid filled 33.3% (44.2 ml) of the volume ofthe two-phase closed thermosyphon. Three heating power levels (200, 300, and 400 W) were used in the experiments with three different flow rates of cooling water (5, 7.5, and 10 g/s) used in the condenser for cooling the system. A increase of 26.39% was achieved in the efficiency of the two-phase closed thermosyphon when 4% (wt) fly ash containing nanofluid was used to replace deionized water at a heat load of 200 W and with a cooling water flow rate of 5 g/s.     

Particle agglomeration and properties of nanofluids

The present study demonstrates the importance of actual agglomerated particle size in the nanofluid and its effect on the fluid properties. The current work deals with 5 to 100 nm nanoparticles dispersed in fluids that resulted in 200 to 800 nm agglomerates. Particle size distributions for a range of nanofluids are measured by dynamic light scattering (DLS). Wet scanning electron microscopy method is used to visualize agglomerated particles in the dispersed state and to confirm particle size measurements by DLS. Our results show that a combination of base fluid chemistry and nanoparticle type is very important to create stable nanofluids. Several nanofluids resulted in stable state without any stabilizers, but in the long term had agglomerations of 250 % over a 2 month period. The effects of agglomeration on the thermal and rheological properties are presented for several types of nanoparticle and base fluid chemistries. Despite using nanodiamond particles with high thermal conductivity and a very sensitive laser flash thermal conductivity measurement technique, no anomalous increases of thermal conductivity was measured. The thermal conductivity increases of nanofluid with the particle concentration are as those predicted by Maxwell and Bruggeman models. The level of agglomeration of nanoparticles hardly influenced the thermal conductivity of the nanofluid. The viscosity of nanofluids increased strongly as the concentration of particle is increased; it displays shear thinning and is a strong function of the level of agglomeration. The viscosity increase is significantly above of that predicted by the Einstein model even for very small concentration of nanoparticles.     

Fabrication of Fe/Fe<Subscript>3</Subscript>C-functionalized carbon nanotubes and their electromagnetic and microwave absorbing properties

Fe/Fe₃C-functionalized carbon nanotubes (CNTs) have been prepared by the floating catalyst chemical vapor-deposition method. It is demonstrated that the Fe and Fe₃C nanostructures are both encapsulated in the CNTs or decorated on the surface of CNTs. The Fe/Fe₃C content in the composites can easily be adjusted by changing the ferrocene concentration in the preparation. The electromagnetic properties of the CNTs have been evaluated in the frequency range of 2–18 GHz, and the nanocomposites exhibit excellent microwave absorbing performance. The CNT composites with higher Fe/Fe₃C content show enhanced microwave reflection losses. The significant influence of the Fe/Fe₃C nanostructures on the microwave absorption is realized by tuning the characteristic impedance of the nanocomposites. With increasing thickness, the maximum reflection loss peak shifts to lower frequency. The microwave absorbing performance of the composites is mainly caused by dielectric loss, resulting from the continuous CNT networks with excellent electrical conductivity.     

Effects of ultrasonication on the properties of maize starch/stearic acid/ sodium carboxymethyl cellulose composite film

Ultrasonic treatment can improve the compatibility between a hydrophobic material and a hydrophilic polymer. The light transmittance, crystalline structure, microstructure, surface morphology, moisture barrier, and mechanical properties of a composite film with or without ultrasonication were investigated. Ultrasound increases the film’s light transmittance, resulting in a film that has good transparency. Ultrasonication did not change the crystalline structure of the polymer film, but promoted V-type complex formation. The surface of the film became smooth and homogeneous after the film-form suspension underwent ultrasonic treatment. Compared to the control film, after ultrasonication at 70% amplitude with a duration of 30 min, the average roughness and maximum roughness declined from 212 nm to 17.6 nm and from 768.7 nm to 86.5 nm, respectively. The composite film with ultrasonication exhibited better tensile and moisture barrier properties than the nonsonicated film. However, long-term and strong ultrasonication will destroy the polymer structure to some extent.     

Sonochemical activation-assisted biosynthesis of Au/Fe3O4 nanoparticles and sonocatalytic degradation of methyl orange

In this research, a sonochemical activation-assisted biosynthesis of Au/Fe₃O₄ nanoparticles is proposed. The proposed synthesis methodology incorporates the use of Piper auritum (an endemic plant) as reducing agent and in a complementary way, an ultrasonication process to promote the synthesis of the plasmonic/magnetic nanoparticles (Au/Fe₃O₄). The synergic effect of the green and sonochemical synthesis favors the well-dispersion of precursor salts and the subsequent growth of the Au/Fe₃O₄ nanoparticles.The hybrid green/sonochemical process generates an economical, ecological and simplified alternative to synthesizing Au/Fe₃O₄ nanoparticles whit enhanced catalytic activity, pronounced magnetic properties. The morphological, chemical and structural characterization was carried out by high- resolution Scanning electron microscopy (HR-SEM), Energy Dispersive X-Ray Spectroscopy (EDS) and X-Ray diffraction (XRD), respectively. Ultraviolet–visible (UV–vis) and X-ray photoelectron (XPS) spectroscopy confirm the Au/Fe₃O₄ nanoparticles obtention. The magnetic properties were evaluated by a vibrating sample magnetometer (VSM). Superparamagnetic behavior, of the Au/ Fe₃O₄ nanoparticles was observed (M_s = 51 emu/g and H_c = 30 Oe at 300 K). Finally, the catalytic activity was evaluated by sonocatalytic degradation of methyl orange (MO). In this stage, it was possible to achieve a removal percentage of 91.2% at 15 min of the sonocatalytic process (160 W/42 kHz). The initial concentration of the MO was 20 mg L⁻¹, and the Fe3O4-Au dosage was 0.075 gL⁻¹. The MO degradation process was described mathematically by four kinetic adsorption models: Pseudo-first order model, Pseudo-second order model, Elovich and intraparticle diffusion model.     

Natural convective heat transfer of Ag-water nanofluid flow inside enclosure with center heater and bottom heat source

A numerical study on natural convective heat transfer inside an enclosure with center heater using nanofluid has been carried out. The effect of different length of center heater on the flow and temperature fields is analysed for different Rayleigh numbers. Results are displayed in terms of streamlines, isotherms, mid height velocity profile and average Nusselt number. The numerical results reveal heat transfer increases with increasing heater length at both vertical and horizontal positions for increasing values of Rayleigh numbers. In particular, a higher increase in heat transfer is obtained with heater situated with vertical position of maximum length. Also it is obtained that enhancement of heat transfer is high for Ag - water nanofluid than CuO -water and Al₂O₃ -water nanofluids.     

Computational analysis of factors influencing thermal conductivity of nanofluids

Numerical investigations are conducted to study the effect of factors such as particle clustering and interfacial layer thickness on thermal conductivity of nanofluids. Based on this, parameters including Kapitza radius and fractal and chemical dimension which have received little attention by previous research are rigorously investigated. The degree of thermal enhancement is analyzed for increasing aggregate size, particle concentration, interfacial thermal resistance, and fractal and chemical dimensions. This analysis is conducted for water-based nanofluids of Alumina (Al₂O₃), CuO, and Titania (TiO₂) nanoparticles where the particle concentrations are varied up to 4 vol%. Results from the numerical work are validated using available experimental data. For the case of aggregate size, particle concentration, and interfacial thermal resistance, the aspect ratio (ratio of radius of gyration of aggregate to radius of primary particle, R _g/a) is varied from 2 to 60. It was found that the enhancement decreases with interfacial layer thickness. Also the rate of decrease is more significant after a given aggregate size. For a given interfacial resistance, the enhancement is mostly sensitive to R _g/a < 20 indicated by the steep gradients of data plots. Predicted and experimental data for thermal conductivity enhancement are in good agreement. On the influence of fractal and chemical dimensions (d _l and d _f) of Alumina–water nanofluid, the R _g/a was varied from 2 to 8, d _l from 1.2 to 1.8, and d _f from 1.75 to 2.5. For a given concentration, the enhancement increased with the reduction of d _l or d _f. It appears a distinctive sensitivity of the enhancement to d _f, in particular, in the range 2–2.25, for all values of R _g/a. However, the sensitivity of d _l was largely depended on the value of R _g/a. The information gathered from this study on the sensitivity of thermal conductivity enhancement to aggregate size, particle concentration, interfacial resistance, and fractal and chemical dimensions will be useful in manufacturing highly thermally conductive nanofluids. Further research on the refine cluster evolution dynamics as a function of particle-scale properties is underway.     

Pyridine-thermal synthesis and high catalytic activity of CeO2/CuO/CNT nanocomposites

Carbon nanotubes (CNTs) were controllably coated with the uninterrupted CuO and CeO₂ composite nanoparticles by a facile pyridine-thermal method and the high catalytic performance for CO oxidation was also found. The obtained nanocomposites were characterized by transmission electron microscopy, scanning electron microscopy, X-ray diffraction as well as X-ray photoelectron spectroscopy. It is found that the CuO/CeO₂ composite nanoparticles are distributed uniformly on the surface of CNTs and the shell of CeO₂/CuO/CNT nanocomposites is made of nanoparticles with a diameter of 30-60 nm. The possible formation mechanism is suggest as follows: the surface of CNTs is modified by the pyridine due to the π-π conjugate role so that the alkaline of pyridine attached on the CNT surface is more enhanced as compared to the one in the bulk solvent, and thus, these pyridines accept the proton from the water molecular preferentially, which result in the formation of the OH⁻ ions around the surface of CNTs. Subsequently, the metal ions such as Ce³⁺ and Cu²⁺ in situ react with the OH⁻ ions and the resultant nanoparticles deposit on the surface of CNTs, and finally the CeO₂/CuO/CNT nanocomposites are obtained. The T₅₀ depicting the catalytic activity for CO oxidation over CeO₂/CuO/CNT nanocomposites can reach ∼113 °C, which is much lower than that of CeO₂/CNT or CuO/CNT nanocomposites or CNTs.     

Synthesis of carbon nanotubes via Fe-catalyzed pyrolysis of phenolic resin

Carbon nanotubes (CNTs) with 40–100 nm in diameter and tens of micrometers in length were prepared via catalytic pyrolysis of phenol resin in Ar at 673–1273 K using ferric nitrate as a catalyst precursor. Structure and morphology of pyrolyzed resin were characterized by X-ray diffraction (XRD), scanning electron microscopy (SEM), transmission electron microscopy (TEM) and Raman spectroscopy. Ferric nitrate was transformed to Fe₃O₄ at 673 K, and to metallic Fe and Fe_xC carbide at 873–1273 K. The optimal weight ratio of Fe catalyst to phenol resin for growing CNTs was 1.00 wt%, and the optimal temperature was 1073 K. In addition, use of a high pressure increased the yield of CNTs. Density functional theory (DFT) calculations suggest that Fe catalysts facilitate the CNTs growth by increasing the bond length and weakening the bond strength in C₂H₄ via donating electrons to the C atoms in it.     

Electrostatic self-assembly of Fe3O4 nanoparticles on carbon nanotubes

Carbon nanotubes (CNTs)-based magnetic nanocomposites can find numerous applications in nanotechnology, integrated functional system, and in medicine owing to their great potentialities. Herein, densely distributed magnetic Fe₃O₄ nanoparticles were successfully attached onto the convex surfaces of carbon nanotubes (CNTs) by an in situ polyol-medium solvothermal method via non-covalent functionalization of CNTs with cationic surfactant, cetyltrimethylammonium bromide (CTAB), and anionic polyelectrolyte, poly(sodium 4-styrenesulfonate) (PSS), through the polymer-wrapping technique, in which the negatively charged PSS-grafted CNTs can be used as primer for efficiently adsorption of positively metal ions on the basis of electrostatic attraction. X-ray diffractometry (XRD), X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) analysis have been used to study the formation of Fe₃O₄/CNTs. The Fe₃O₄/CNTs nanocomposites were proved to be superparamagnetic with saturation magnetization of 43.5 emu g^?1. A mechanism scheme was proposed to illustrate the formation process of the magnetic nanocomposites.