Absorption performance enhancement by nano-particles and chemical surfactants in binary nanofluids

The objectives of this paper are to visualize the bubble behavior during the NH₃/H₂O absorption process with chemical surfactant and nano-particles and to study the effect of nano-particles and surfactants on the absorption characteristics. Binary nanofluid which means binary mixture with nano-sized particles is tested to apply nanofluid to the absorption system. Cu, CuO and Al₂O₃ nano-particles are added into NH₃/H₂O solution to make the binary nanofluids, and 2-ethyl-1-hexanol, n-octanol and 2-octanol are used as the surfactants. The concentration of ammonia in the basefluid, that of nano-particles in the nanofluid, and that of surfactants in the nanofluid are considered as the key parameters. The results show that the addition of surfactants and nano-particles improves the absorption performance up to 5.32 times. It can be concluded that the addition of both surfactants and nano-particles enhances significantly the absorption performance during the ammonia bubble absorption process.     

Heat and mass transfer enhancement of binary nanofluids for H2O/LiBr falling film absorption process

The objectives of this study are to measure the vapor absorption rate and heat transfer rate for falling film flow of binary nanofluids, and to compare the enhancement of heat transfer and mass transfer under the same conditions of nanofluids. The key parameters are the base fluid concentration of LiBr, the concentration of nanoparticles in weight %, and nanoparticle constituents. The binary nanofluids are H₂O/LiBr solution with nanoparticles of Fe and Carbon nanotubes (CNT) with the concentrations of 0.0, 0.01 and 0.1 wt %. The vapor absorption rate increases with increasing the solution mass flow rate and the concentration of Fe and CNT nanoparticles. It is found that the mass transfer enhancement is much more significant than the heat transfer enhancement in the binary nanofluids with Fe and CNT. It is also found that the mass transfer enhancement from the CNT nanoparticles becomes higher than that from the Fe nanoparticles. Therefore, the CNT is a better candidate than Fe nanoparticles for absorption performance enhancement in H₂O/LiBr absorption system.     

Experimental study on enhancement of ammonia-water falling film absorption by adding nano-particles

Based on the preparation of Al₂O₃, Fe₂O₃ and ZnFe₂O₄ nanofluid, the comparative experiments on the falling film absorption between ammonia-water and ammonia-water with various kinds of nano-particles are carried out. Experimental results show that the sorts and mass fraction of nano-particles, the viscosity and stability of nanofluid, as well as the mass fraction of ammonia in the basefluid are considered as the key parameters. The absorption of ammonia is weakened by only adding surfactants or adding poorly dispersed nano-particles. The increase of mass fraction of nano-particles with matched surfactants can improve the absorption rate of ammonia under the condition that the viscosity of nanofluid does not increase remarkably, and there is an optimal mass fraction for each kind of nano-particles and surfactant. With the increase in ammonia mass fraction of initial nanofluid, the absorption potential capacity decline, but the enhancing effect induced by the nanofluid is more obvious compared to that without nano-particles. The effective absorption ratio can be increased by 70% and 50% with Fe₂O₃ and ZnFe₂O₄ nanofluid respectively when the initial ammonia mass fraction is 15%. The absorption enhancement by the nanofluid is attributable to the heat transfer enhancement and the decrease in viscosity of nanofluid, which are strongly proved by the temperature differences in cooling water and nanofluids as well as the falling film flowing time.     

The effect of chemical surfactants on the absorption performance during NH3/H2O bubble absorption process

The objectives of this paper are to visualize the bubble behavior by shadow graphic method, to examine the effect of surfactants on the bubble type absorption, and to find the optimal conditions to design highly effective compact absorber for NH₃/H₂O absorption system. The initial concentrations of NH₃/H₂O solution and the kinds and the concentrations of surfactants are considered as key parameters. By measuring the absorption rate for each condition, two effects of the addition of surfactants, the Marangoni and the barrier effect, are compared with each other. The results show that the addition of surfactant enhances the absorption performance up to 4.81 times. The experimental correlations of the effective absorption ratio for each surfactant, 2-ethyl-1-hexanol, n-octanol, and 2-octanol, are suggested within ±15, ±10, and ±10%, respectively.     

The effect of heat transfer additive and surface roughness of micro-scale hatched tubes on absorption performance

The objectives of this paper are to investigate the effect of heat transfer additive and surface roughness of micro-scale hatched tubes on the absorption performance and to provide a guideline for the absorber design. Two different micro-scale hatched tubes and a bare tube are tested to quantify the effect of the surface roughness on the absorption performance. The roughness of the micro-scale hatched tubes ranges 0.39–6.97 μm. The working fluid is H₂O/LiBr solution with inlet concentration of 55, 58 and 61 wt.% of LiBr. Normal Octanol is used as the heat transfer additive with the concentration of 400 ppm. The absorber heat exchanger consists of 24 horizontal tubes in a column, liquid distributor at the liquid inlet and the liquid reservoir at the bottom of the absorber. The effect of heat transfer additive on the heat transfer rate is found to be more significant in the bare tube than that in the micro-scale hatched tubes. It is found that the absorption performance for the micro-hatched tube with heat transfer additive becomes up to 4.5 times higher than that for the bare tube without heat transfer additive. It is concluded that the heat transfer enhancement by the heat transfer additive is more significant than that by the micro-scale surface treatment.     

Effect of vapor flow on the falling-film heat and mass transfer of the ammonia/water absorber

Falling-film heat and mass transfer in an absorber can be influenced by the motion of the surrounding refrigerant vapor. In this study, the effect of the vapor flow direction on the absorption heat and mass transfer has been investigated for a falling-film helical coil absorber which is frequently used in the ammonia/water absorption refrigerators. The heat and mass transfer performance was measured for both parallel and countercurrent flow. The experiments were carried out for three different solution concentrations (3, 14, and 30%). The vapor in equilibrium with the solution is supplied to the test section. It is found that the falling-film heat and mass transfer is deteriorated in the countercurrent flow if the specific volume of the vapor solution is large. For the countercurrent flow, the high velocity of the vapor due to large specific volume seems to cause the unfavorable distribution of falling-film and reduce the heat and mass transfer performance of the ammonia absorber. The effect of vapor flow direction decreased with increasing concentration of ammonia solution since the specific volume of the ammonia vapor which is in equilibrium with the solution becomes smaller and the vapor velocity becomes lower.     

A phenomenological theory of polycomponent interactions in non-ideal mixtures. Application to NH3/H2O and other working pairsInteractions entre les composants de mélanges non-idéaux : théorie et application au fluide actif NH3 / H2O et à d'autres fluides actifs

The paper proposes an original linear phenomenological theory (Ph T) of evolution physical mono-, bi- and particular polycomponent gas–liquid interactions with non-ideal mixture. The expressions of the phenomenological factors (entropy source, force, coefficient and coupled heat and mass transfer currents) are deduced. The theory is particularized to the NH₃/H₂O and other gas–liquid systems used in the thermal absorption technology. The work's conclusions are listed next. The paper raises the problem of ammonia bubble absorption which is difficult to answer with current theory of interface mass transfer and absorption as a surface phenomenon. The heat and mass transfer at the gas–liquid interface is governed by the thermodynamic force, which applies also to solid–liquid, solid–gas, or liquid–liquid, gas–gas type interactions and continuous or discontinuous media. The paper mentions a postulate referring to the force behavior approaching an ideal point, previously formulated by the author. According to its consequence, the mass and heat currents suffer an ideal point approaching (i.p.a.) effect, not mentioned so far in the specialized literature, consisting in a continuous increase of their absolute value by several percent (for a pure component), to several hundred times (for a binary system) when the interacting system approaches an ideal state, as compared to the values of states which are far from the same ideal point. In this way, “far from equilibrium” becomes synonymous to “low interaction”. The classic assessment of the interface mass transfer by analogy with heat transfer lacks basic physics. The (Ph T) satisfactorily explains the problem of ammonia bubble absorption. Absorption is a mass phenomenon, not a surface one. An intensive way of improving absorption is emphasized, which seeks to promote the i.p.a. effect appearance rather than the extensive way currently used, based on increasing gas–liquid interaction area. To this extent, the bubble absorber is hereby proposed for efficient absorption. The i.p.a. effect existence offers an additional chance for a satisfactory explanation of the Marangoni effect.     

Absorption of water vapour into lithium bromide-based solutions with additives using a simple stagnant pool absorberAdsorption de la vapeur d'eau par des solutions à base de bromure de lithium à l'aide d'un absorbeur simple de type à surface liquide stagnante

Absorption of water vapour into the 50 mass % lithium bromide solution with four eight-carbon alcohol additives such as n-octanol, 2-octanol, 3-octanol, and 2-ehtyl-1-hexanol were investigated by using a simple stagnant pool absorber. Four solutions of the 60 mass % lithium bromide + water, 68 mass % lithium bromide + ethylene glycol + water (LiBr/HO(CH₂)₂OH = 4.5 by mass), 60 mass % lithium bromide + lithium iodide + water (LiBr/Lil = 4 by mole), and 70 mass % lithium bromide + zinc chloride + water (LiBr/ZnCl₂ = 1 by mass) containing the 2-ethyl-1-hexanol additive were also considered to examine the additive effect on mass transfer of water vapour into the different types of absorbents. The experimental apparatus could be used with good confidence and accuracy particularly for studying mass transfer enhancement over the effective range of additive concentration which, in this work, is mostly between 10 and 500 ppm. A vigorous interfacial turbulence was observed during absorption process using additives. The water vapour absorption rate remarkably increased with increasing the additive concentrations up to about 200 ppm and then stopped increasing above 200 ppm for all the systems considered. The onset additive concentrations for enhancing mass transfer were located between 5 and 8 ppm for all systems except two systems of the 50 mass % lithium bromide solution with 3-octanol and 70 mass % lithium bromide + zinc chloride solution with 2-ethtyl-1-hexanol for which the corresponding concentrations were 2.5 and 35 ppm, respectively.     

Spray absorbers in absorption systems using lithium nitrate–ammonia solution

In the present work, the spray absorption method is studied for the absorption of ammonia refrigerant vapour by lithium nitrate–ammonia solutions. Mass transfer coefficients attainable using the spray absorption method are estimated. In this study the low-pressure absorber of a double-stage absorption refrigeration system is considered. Results show that the mass transferred is maximum (about 60% of the total) during the deceleration period of the drops. This period represents about 13.4% of the time required to reach the equilibrium state at the end of the absorption chamber. The results show that a time-average mass transfer coefficient equal to k_m=18.6×10⁻⁵ m s⁻¹ may be attained.     

Analytical investigation of two different absorption modes: falling film and bubble types

The objectives of this paper are to analyze a combined heat and mass transfer for an ammonia–water absorption process, and to carry out the parametric analysis to evaluate the effects of important variables such as heat and mass transfer areas on the absorption rate for two different absorption modes — falling film and bubble modes. A plate heat exchanger with an offset strip fin (OSF) in the coolant side was used to design the falling film and the bubble absorber. It was found that the local absorption rate of the bubble mode was always higher than that of the falling film model leading to about 48.7% smaller size of the heat exchanger than the falling film mode. For the falling film absorption mode, mass transfer resistance was dominant in the liquid flow while both heat and mass transfer resistances were considerable in the vapor flow. For the bubble absorption mode, mass transfer resistance was dominant in the liquid flow while heat transfer resistance was dominant in the vapor region. Heat transfer coefficients had a more significant effect on the heat exchanger size (absorption rate) in the falling film mode than in the bubble mode, while mass transfer coefficients had a more significant effect in the bubble mode than in the falling film mode.     

A study on numerical simulations and experiments for mass transfer in bubble mode absorber of ammonia and water

An absorber is a major component in the absorption refrigeration systems, and its performance greatly affects the overall system performance. In this study, both the numerical and experimental analyses in the absorption process of a bubble mode absorber were performed. Gas was injected into the bottom of the absorber at a constant solution flow rate. The region of gas absorption was estimated by both numerical and experimental analyses. A higher gas flow rate increases the region of gas absorption. As the temperature and concentration of the input solution decrease, the region of gas absorption decreases. In addition, the absorption performance of the countercurrent flow was superior to that of cocurrent. Mathematical modeling equations were derived from the material balance for the gas and liquid phases based on neglecting the heat and mass transfer of water from liquid to gas phase. A comparison of the model simulation and experimental results shows similar values. This means that this numerical model can be applied for design of a bubble mode absorber.     

Heat transfer enhancement by Marangoni convection in the NH3–H2O absorption process

The objectives of this paper are to quantify the effect of Marangini convection on the absorption performance for the ammonia–water absorption process, and to visualize Marangoni convection that is induced by adding a heat transfer additive, n-octanol. A real-time single-wavelength holographic interferometer is used for the visualization using a He–Ne gas laser. The interface temperature is always the highest due to the absorption heat release near the interface. It was found that the thermal boundary layer (TBL) increased faster than the diffusion boundary layer (DBL), and the DBL thickness increased by adding the heat transfer additive. At 5 s after absorption started, the DBL thickness for 5 mass% NH₃ without and with the heat transfer additive was 3.0 and 4.5 mm, respectively. Marangoni convection was observed near the interface only in the cases with heat transfer additive. The Marangoni convection was very strong just after the absorption started and it weakened as time elapsed. It was concluded that the absorption performance could be improved by increasing the absorption driving potential (x_vb−x_vi) and by increasing the heat transfer additive concentration. The absorption heat transfer was enhanced as high as 3.0–4.6 times by adding the heat transfer additive that generated Marangoni convection.     

Interfacial mass transfer and mass transfer coefficient in aqua ammonia packed bed absorberTransfert de masse à l'interface et coéfficient de transfert de masse dans un absorbeur à matelas dispersant eau–ammoniac

A mathematical model was given to predict the mass transfer between flow of a mixture of ammonia vapor and water vapor and a flow of aqua ammonia solution at any interface within a packed bed absorber (PBA). The model used the molal mass and heat transfer coefficients in both the liquid and gas phases, the interface molal solution concentration, interface molal vapor mixture concentration, interface temperature, and the heat transfer coefficients in the liquid and gas phases in both sides of the interface. The heat transfer coefficient was corrected to account for the mass transfer. The model was also used to derive a convenient mass transfer coefficient which was based on the bulk mass concentration, not on the molal concentration, and not directly dependent on the concentration at the interface. To complete the model, mathematical correlations were derived for several thermodynamic and physical properties of aqua ammonia solution and vapor mixture. A computer program was developed to demonstrate the use of the model to predict the rate of absorption of ammonia vapor at an interface within the packed bed at various operating conditions.     

The role of surfactant adsorption rate in heat and mass transfer enhancement in absorption heat pumps

The importance of heat and mass transfer additives in absorption chillers and heat pumps has been recognized for over three decades. However, a universally accepted model for the mechanisms responsible for enhanced absorption rates has yet to be proposed. The Marangoni effect—an instability arising from gradients in surface tension at the liquid-vapor interface—is generally accepted as the cause of the convective flows that enhance transfer rates. Certain surfactant additives can significantly improve absorption rates and thus reduce the overall transfer area required by a given machine. Any means available that can increase the efficiency and acceptability of absorption machines is to be welcomed, as this technology provides an alternative to vapor compression systems which is both environmentally friendly and more versatile with regards to energy sources. This study investigates the rate at which a surfactant additive adsorbs at a liquid-vapor interface. The residence time of the falling liquid solution in an absorber is quite short. An effective additive must not only reduce the surface tension of the solution; it must do so quickly enough to cause the Marangoni instability within the short absorption process time. The entrance region of an absorber features a freshly exposed interface at which no surfactant has adsorbed. A numerical model is used to analyze surfactant relaxation rates in a static film of additive-laced solution. Kinetic parameters for the combination of the working pair LiBr-H₂O and the additive 2-ethyl-1-hexanol are derived from data in the literature for static and dynamic surface tension measurements. Bulk, interfacial and boundary parameters influencing relaxation rates are discussed for surfactant adsorption occurring in the absence of absorption, as well as for concurrent adsorption and stable vapor absorption. Initial solution conditions and absorption driving force are shown to impact the potential for instability in the effect they have on the rate of interfacial additive adsorption.     

Development of a slug flow absorber working with ammonia–water mixture: part II—data reduction model for local heat and mass transfer characterization

This study deals with a data reduction model for clarifying experimental results of a counter-current slug flow absorber, working with ammonia–water mixture, for significantly low solution flow rate conditions. The data reduction model to obtain the local heat and mass transfer coefficient on the liquid side is proposed by using the drift flux model to analyze the flow characteristics. The control volume method and heat and mass transfer analogy are employed to solve the combined heat and mass transfer problem. As a result, it is found that the local heat and mass transfer coefficient on the liquid side of the absorber is greatly influenced by the flow pattern. The heat and mass transfer coefficient at the frost flow region is higher than that at the slug flow region due to flow disturbance and random fluctuation. The solution flow rate and gas flow rate have influence on the local heat and mass transfer coefficient at the frost flow region. However, it is insignificant at the slug flow region.     

Mass transfer correlation of NH3–H2O bubble absorption

The objectives of this paper are to study the effect of key parameters on absorption performance and to develop an experimental correlation of mass transfer coefficient for ammonia–water bubble absorption. The orifice diameter, liquid concentration and vapor velocity are considered as the key parameters. This study successfully visualized the bubble behavior and measured the volumetric diameter of bubbles during the bubble absorption process. The bubble absorption is grouped into two processes, bubble growth (process I) and bubble disappearance (process II), respectively. The following conclusions were drawn from the present study. A new experimental correlation for the volumetric bubble diameter was proposed with ±15% error band, which could be applied to calculate the mass transfer coefficient. The mass transfer coefficient increased with a decrease of the liquid concentration. In process II, the mass transfer coefficient increased with an increase of the Galileo number. Finally, experimental correlations of mass transfer coefficient were developed for processes I and II with ±18% error bands.     

Development of a slug flow absorber working with ammonia-water mixture: part I—flow characterization and experimental investigation

This study deals with an experimental investigation for a counter-current slug flow absorber, working with ammonia–water mixture, for significantly low solution flow rate conditions that are required for operating as the GAX (generator absorber heat exchanger) cycle. It is confirmed that the slug flow absorber operates well at the low solution flow rate conditions. From visualization results of the flow pattern, frost flow just after the gas inlet, followed by slug flow with well-shaped Taylor bubble, is observed, while dry patch on the tube wall are not observed. The liquid film at the slug flow region has smooth gas–liquid interface structure without apparent wavy motion. The local heat transfer rate is measured by varying main parameters, namely, ammonia gas flow rate, solution flow rate, ammonia concentration of inlet solution and coolant inlet conditions. The heat transfer rate while absorption is taking place is higher than that after absorption has ended. The absorption length is greatly influenced by varying main parameters, due to flow conditions and thermal conditions.     

Experimental correlation of falling film absorption heat transfer on micro-scale hatched tubes

The objectives of this paper are to investigate the effect of surface roughness of micro-hatching tubes on the absorption performance and to develop an experimental correlation of Nusselt number as a function of the roughness. Two different micro-scale hatched tubes and a bare tube are tested to quantify the effect of the surface roughness on the absorption performance. The roughness of the micro-scale hatched tubes ranges 0.386–11.359 μm. The working fluid is H₂O/LiBr solution with inlet concentration of 55, 58 and 61 wt.% of LiBr. The absorber heat exchanger consists of 24 horizontal tubes in a column, liquid distributor at the liquid inlet and the liquid reservoir at the bottom of the absorber. It was found that absorption performance of micro-hatching tubes was improved up to two times compared with the bare tube. An experimental correlation of Nusselt number was developed as a function of the film Reynolds number and the roughness with an error band of ±25%.     

The effect of nano-particles on the bubble absorption performance in a binary nanofluid

The objectives of this paper are to examine the effect of nano particles on the bubble type absorption by experiment and to find the optimal conditions to design highly effective compact absorber for NH₃/H₂O absorption system. The initial concentrations of NH₃/H₂O solution and the kinds and the concentrations of nano particles are considered as key parameters. The results show that the addition of nano particles enhances the absorption performance up to 3.21 times. Moreover, the absorption rate increases with increasing concentration of nano particles and the nano particles are more effective for lower absorption potential solution. The potential enhancement mechanism for binary nanofluid is suggested. The experimental correlations of the effective absorption ratio for each nano particles, Cu, CuO, and Al₂O₃, are suggested within ±10% error-band.     

Coupled heat and mass transfer during nonisothermal absorption by falling droplet with internal circulation

We considered mass and heat transfer during nonisothermal absorption of a gas by a falling droplet with internal circulation. Gas phase is assumed to be free of inert admixtures and mass transfer is liquid phase controlled. Mass flux is directed from a gaseous phase to a droplet, and the interfacial shear stress causes a fluid flow inside the droplet. Droplet deformation under the influence of interface shear stress is neglected. Absorbate accumulation and temperature increase in the bulk of liquid phase are taken into account. The problem is solved in the approximations of a thin concentration and temperature boundary layers in the liquid phase. The thermodynamic parameters of the system are assumed constant. The system of transient partial parabolic differential equations of convective diffusion and energy balance with time-dependent boundary conditions is solved by combining the similarity transformation method with Duhamel's theorem, and the solution is obtained in a form of Volterra integral equation of the second kind which is solved numerically. Theoretical results are compared with available experimental data for water vapor absorption by falling droplets of aqueous solution of LiBr.