Membrane materials and modification for thermal induced membrane separation processes

Author(s):  
Mihir Kumar Purkait ◽  
Randeep Singh ◽  
Piyal Mondal ◽  
Dibyajyoti Haldar
Author(s):  
Mihir Kumar Purkait ◽  
Randeep Singh ◽  
Piyal Mondal ◽  
Dibyajyoti Haldar

2013 ◽  
Vol 333 ◽  
pp. 135-147 ◽  
Author(s):  
Ahmad Abdul Latif ◽  
Jimoh K. Adewole ◽  
Suzylawati Binti Ismail ◽  
Leo Choe Peng ◽  
Abdullah S. Sultan

Natural gas (NG) processing and membrane technology are two very important fields that are of great significance due to increasing demand for energy as well as separation of gas mixtures. While NG is projected to be the number one primary source of energy by 2050, membrane separation is a commercially successful competitor to other separation techniques for energy efficient gas separation processes [1]. Most of the NG produced in the world is coproduced with acid gases such as CO2which need to be removed to increase the caloric value of NG. A comprehensive review of research efforts in CO2separation from natural gas is required to capture details of the current scientific and technological progresses on the development of new membrane materials with better separation performance, and the improvement of properties of the existing ones. This paper presents the progress that has been achieved in eliminating the limitations that dominate the large scale application of membrane materials at the present time. Various polymers that have been developed to resist plasticization and the method employed to fabricate these polymers are highlighted. Also the range of plasticization pressures (together with corresponding selectivities and permeabilities at these pressures) that have so far been achieved by these fabrication methods is presented. It is believed that this review will serve as a good reference source especially for research in design and development of membrane materials with better resistance to CO2-induced plasticization.


Author(s):  
Mihir Kumar Purkait ◽  
Randeep Singh ◽  
Piyal Mondal ◽  
Dibyajyoti Haldar

Author(s):  
Mihir Kumar Purkait ◽  
Randeep Singh ◽  
Piyal Mondal ◽  
Dibyajyoti Haldar

Author(s):  
Mihir Kumar Purkait ◽  
Randeep Singh ◽  
Piyal Mondal ◽  
Dibyajyoti Haldar

Membranes ◽  
2020 ◽  
Vol 10 (11) ◽  
pp. 328
Author(s):  
Chiara Muzzi ◽  
Alessio Fuoco ◽  
Marcello Monteleone ◽  
Elisa Esposito ◽  
Johannes C. Jansen ◽  
...  

Global warming by greenhouse gas emissions is one of the main threats of our modern society, and efficient CO2 capture processes are needed to solve this problem. Membrane separation processes have been identified among the most promising technologies for CO2 capture, and these require the development of highly efficient membrane materials which, in turn, requires detailed understanding of their operation mechanism. In the last decades, molecular modeling studies have become an extremely powerful tool to understand and anticipate the gas transport properties of polymeric membranes. This work presents a study on the correlation of the structural features of different membrane materials, analyzed by means of molecular dynamics simulation, and their gas diffusivity/selectivity. We propose a simplified method to determine the void size distribution via an automatic image recognition tool, along with a consolidated Connolly probe sensing of space, without the need of demanding computational procedures. Based on a picture of the void shape and width, automatic image recognition tests the dimensions of the void elements, reducing them to ellipses. Comparison of the minor axis of the obtained ellipses with the diameters of the gases yields a qualitative estimation of non-accessible paths in the geometrical arrangement of polymeric chains. A second tool, the Connolly probe sensing of space, gives more details on the complexity of voids. The combination of the two proposed tools can be used for a qualitative and rapid screening of material models and for an estimation of the trend in their diffusivity selectivity. The main differences in the structural features of three different classes of polymers are investigated in this work (glassy polymers, superglassy perfluoropolymers and high free volume polymers of intrinsic microporosity), and the results show how the proposed computationally less demanding analysis can be linked with their selectivities.


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