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10篇 您的检索式:作者名="Moghadassi"
    题名 作者 年代 出处 被引量
1Experimental study of hydrogen sulfide hydrate formation: Induction time in the presence and absence of kinetic inhibitor显示文摘In this paper, the effect of adding different concentrations of kinetic inhibitors on the induction time of hydrogen sulfide hydrate formation in a reactor equipped with automatic adjustable temperature controller is studied. A novel method namely 'sudden cooling' is used for performing the relevant measurements, in which the induction time of H2S hydrate in the presence/absence of PVP and L-tyrosine with different concentrations (100, 500, and 1000 ppm) is determined. As a result, PVP with the concentration of 1000 ppm in aqueous solution is detected as a more suitable material for increasing the induction time of H2S hydrate formation among the investigated kinetic hydrate inhibitors.Yousef Salamat Abdolreza Moghadassi Mohammad Illbeigi Ali Eslamimanesh Amir H. Mohammadi 2013Journal of Energy Chemistry2013,22,1:4
2Numerical simula- tion of mass transfer in gas-liquid hollow fiber membrane contactors for laminar flow conditions 显示文摘Shirazian S Moghadassi A Moradi S 2009Simulation Modelling Practice and Theory2009,17,4:1
3Numerical simulation of mass transfer in gas-liquid hollow fiber membrane contactors for laminar flow conditions显示文摘Shirazian S Moghadassi A Moradi S 2009Simul Model Pract Th2009,17,4:1
4Effect of CuO nanoparticles in enhancing the thermal eonductivities of monoethylene glycol and paraffin fluids 显示文摘MOGHADASSI A R HOSSEINI S M HENNEKE D E 2010Ind & Eng Chem Res2010,49,:1
5The application of the discrete lumped kinetic approach for the modeling of a vacuum gas oil hydrocracker Unit显示文摘Moghadassi A R Amini N Fadavi O 2011Petroleum Science and Technology2011,29,23:1
6Numerical simulation of mass transfer in gas-liquid hollow fiber membrane contactors for laminar flow conditions显示文摘Shirazian S Moghadassi A Moradi S 2009Simulation Modelling Practice and Theory2009,17,:1
7A new dimensionless group model for determining the viscosity of nanofluids显示文摘Hosseini S M Moghadassi A R Hcnneke D E 2010Journal of ThermalAnalysis and Calorimetry2010,100,3:1
8Preparation and characterization of aerylonitrile- butadiene -styrene/poly(vinyl acetate) membrane for COg removal 显示文摘Sanaeepur H Amooghin A E Moghadassi A 2011Sep Purif Teehnol2011,80,3:1
9Numerical simulation of mass transfer in gas-liquid hollow fiber membrane contactors for laminar flow conditions显示文摘Shirazian Saeed Moghadassi Abdolreza Moradi Sadegh 0,,:1
10Advances in high carbon dioxide separation performance of poly(ethylene oxide)-based membranes显示文摘Poly(ethylene-oxide)(PEO)-based membranes have attracted much attention recently for CO2 separation because CO2 is highly soluble into PEO and shows high selectivity over other gases such as CH4 and N2.Unfortunately,those membranes are not strong enough mechanically and highly crystalline,which hinders their broader applications for separation membranes.In this review discussions are made,as much in detail as possible,on the strategies to improve gas separation performance of PEO-based membranes.Some of techniques such as synthesis of graft copolymers that contain PEO,cross-linking of polymers and blending with long chains polymers contributed significantly to improvement of membrane.Incorporation of ionic liquids/nanoparticles has also been found effective.However,surface modification of nanoparticles has been done chemically or physically to enhance their compatibility with polymer matrix.As a result of all such efforts,an excellent performance,i.e.,CO2 permeability up to 200 Barrer,CO2/N2 selectivity up to 200 and CO2/CH4 selectivity up to 70,could be achieved.Another method is to introduce functional groups into PEO-based polymers which boosted CO2 permeability up to 200 Barrer with CO2/CH4 selectivity between 40 and 50.The CO2 permeability of PEO-based membranes increases,without much change in selectivity,when the length of ethylene oxide is increased.Samaneh Bandehali Abdolreza Moghadassi Fahime Parvizian Sayed Mohsen Hosseini Takeshi Matsuura Ezatollah Joudaki 2020Journal of Energy Chemistry2020,29,7:0
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