Abstract

Adsorption cooling is getting huge attention from last few years due to environment-friendly and thermally-driven technology. Many systems designs based on various adsorbent-adsorbate pairs are investigated worldwide to develop a cost-effective and high-performance system. Until now, performance of the systems is lower as compared to conventional compressor-based systems. Performance of the adsorption systems mainly depends on adsorption equilibrium, adsorption kinetics, isosteric heat of adsorption, and thermo-physical/chemical properties of assorted adsorbent-refrigerant pairs. Thereby, the present study aims to review and compare the physical properties (surface area, pore volume/size etc.) of adsorbents and adsorption equilibrium (adsorption isotherm) by various types of adsorbent-adsorbate pairs available in the literature. Amount of adsorbate adsorbed per unit mass of adsorbent has been critically reviewed and compared accordingly. Highest adsorption uptake was attributed in case of R-32 adsorption onto phenol resin-based activated carbon i.e. 2.23 kg/kg (excess adsorption) and 2.34 kg/kg (absolute adsorption) at 30 °C and 1670 kPa. Activated carbon of type Maxsorb-III being highly microporous possesses high surface area and shows good adsorption uptakes for most of the adsorbates including ethanol, methanol R-134a, CO2, R-507A and n-butane. In addition, fundamentals, principle and features of adsorption cooling systems are discussed. Adsorption equilibrium models used to express the adsorption mechanics of adsorbent-adsorbate pairs are explored, and the models’ parameters are collectively listed and discussed. The review is useful to prioritize available adsorbent-adsorbate pairs for adsorption based heat transformation applications. The study is useful for researchers working for the development of adsorbent materials for various applications and conditions.

Full Text
Paper version not known

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.