TY - JOUR TI - Density, viscosity and CO2 solubility of novel solvent SP - 301 N1 - cited By 0; Conference of International Conference on Process Engineering and Advanced Materials, ICPEAM 2012 ; Conference Date: 12 June 2012 Through 14 June 2012; Conference Code:106208 AV - none EP - 306 SN - 10226680 PB - Trans Tech Publications Ltd KW - Absorption; EthanolamineS; Gas absorption; Global warming; Loading; Physical properties; Process engineering; Solubility; Solvents; Viscosity KW - 1 amino 2 propanols; Absorption capacity; Acid gas absorption; Elevated pressure; Equilibrium cell; High-pressure condition; Monoethanolamine; Solubility of CO KW - Carbon dioxide ID - scholars5175 N2 - Carbon dioxide (CO2) is the major cause of accelerating global warming. It is importantto employ efficient method to capture CO2. Absorption is the most established technique to separate CO2 and amines are most commonly used as solvent. In this study, density and viscosity of an amine based novel solvent named Stonvent were investigated at temperature ranging from 298.15 K to 338.15 K. CO2 solubility in Stonvent was measured at varying pressures, temperatures and concentrations. The experiments were conducted at temperatures (303.15, 318.15 and 333.15) K, and at pressures (0.5, 1, 1.5 and 3) MPa over a wide range of concentration (10, 20, 30 and 100) mass . Solubility of CO2 was determined from pressure drop due to absorption of CO2 into solvent within equilibrium cell. Absorption capacity of Stonvent increases significantly with increasing pressure. Solubility of CO2 in Stonvent is higher compared to Monoethanolamine (MEA), 1-amino-2-propanol (MIPA) and 2-amino-2-methyl-1,3-propanediol (AMPD) at elevated pressure, hence posing Stonvent as an attractive alternative for acid gas absorption in high pressure conditions. Substantial increase in CO2 loading was observed when concentration of Stonvent is increased and when temperature is decreased. © (2014) Trans Tech Publications, Switzerland. CY - Kuala Lumpur VL - 917 UR - https://www.scopus.com/inward/record.uri?eid=2-s2.0-84904045455&doi=10.4028%2fwww.scientific.net%2fAMR.917.301&partnerID=40&md5=254354758b3e96e540a3998ab64abffc A1 - Kee, W.M. A1 - Shariff, A.M. A1 - Bustam, M.A. A1 - Keong, L.K. A1 - Karikalan, T. A1 - Murshid, G. JF - Advanced Materials Research Y1 - 2014/// ER -