Enhancement of heat and mass transfer in silica-expanded graphite composite blocks for adsorption heat pumps

2000 ◽  
Vol 23 (1) ◽  
pp. 64-73 ◽  
Author(s):  
Tai-Hee Eun ◽  
Hyun-Kon Song ◽  
Jong Hun Han ◽  
Kun-Hong Lee ◽  
Jong-Nam Kim
2021 ◽  
pp. 133365
Author(s):  
Marc Scherle ◽  
Timothy A. Nowak ◽  
Stefan Welzel ◽  
Bastian J.M. Etzold ◽  
Ulrich Nieken

2017 ◽  
Vol 38 (4) ◽  
pp. 191-207 ◽  
Author(s):  
Kinga Kowalska ◽  
Bogdan Ambrożek

Abstract The dynamic performance of cylindrical double-tube adsorption heat pump is numerically analysed using a non-equilibrium model, which takes into account both heat and mass transfer processes. The model includes conservation equations for: heat transfer in heating/cooling fluids, heat transfer in the metal tube, and heat and mass transfer in the adsorbent. The mathematical model is numerically solved using the method of lines. Numerical simulations are performed for the system water-zeolite 13X, chosen as the working pair. The effect of the evaporator and condenser temperatures on the adsorption and desorption kinetics is examined. The results of the numerical investigation show that both of these parameters have a significant effect on the adsorption heat pump performance. Based on computer simulation results, the values of the coefficients of performance for heating and cooling are calculated. The results show that adsorption heat pumps have relatively low efficiency compared to other heat pumps. The value of the coefficient of performance for heating is higher than for cooling


Author(s):  
Ananda Krishna Nagavarapu ◽  
Srinivas Garimella

This paper presents the development of a miniaturization technology for heat and mass exchangers used in absorption heat pumps. The exchanger consists of an array of parallel, aligned alternating shims with integral microscale features, enclosed between cover plates. These microscale features facilitate the flow of the various fluid streams and the associated heat and mass transfer. In an absorber application, effective vapor and solution contact and microscale features for the flow of both the solution and the coolant induce high heat and mass transfer rates without any active or passive surface enhancement. The geometry ensures even flow distribution with minimal overall pressure drops. A model of the coupled heat and mass transfer process for ammonia-water absorbers using this configuration under typical operating conditions demonstrates the potential for extremely small absorption components. The proposed concept is compact, modular, versatile, and in an eventual implementation, can be mass produced. Additionally, the same concept can be extended to the other absorption heat pump components as well as for several other industries involved in multicomponent fluid processes.


Author(s):  
Alex Raymond ◽  
Srinivas Garimella

Adsorption heat pumps and chillers can utilize solar or waste heat to provide space conditioning, process heating or cooling, or energy storage. In these devices, accurate modeling of intraparticle adsorbate mass transfer is an important part of predicting overall performance. The linear driving force (LDF) approximation is often used for modeling intraparticle mass transfer in place of the more detailed Fickian diffusion (FD) equation for its computational simplicity. This paper directly compares the adsorbate contents predicted by the conventional LDF approximation, an empirical LDF approximation proposed by El-Sharkawy et al. [1], and the FD equations for cylindrical adsorbent fibers such as activated carbon fiber (ACF). The conditions under which the LDFs agree with the FD equation are then evaluated. It is shown that for a given working pair, agreement between the LDF and FD equations is affected by the diffusivity, particle radius, half-cycle time, initial adsorbate content, and equilibrium adsorbate content. The maximum possible error in adsorbate content predicted by the LDF approximation compared with the FD solution is then calculated for the ACF (A-20)-ethanol working pair. Although the maximum error will be different for other cases, the technique used in this paper can be reproduced to determine the greatest possible LDF error for any working pair.


2000 ◽  
Author(s):  
Michael S. Koenig ◽  
Gershon Grossman ◽  
Khaled Gommed

Abstract 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.


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