Journal
MATERIALS TODAY CHEMISTRY
Volume 22, Issue -, Pages -Publisher
ELSEVIER SCI LTD
DOI: 10.1016/j.mtchem.2021.100598
Keywords
Comb-like polysiloxane; Membrane; Membrane gas separation; Side chains assembly; Hydrocarbon separation
Funding
- Russian Science Foundation [19-19-00647]
- Russian Science Foundation [19-19-00647] Funding Source: Russian Science Foundation
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The physicochemical properties of comb-like polysiloxanes with different types of side-chain substituents were systematically investigated, revealing the impact on microphase assembly and hydrocarbon transport properties. The presence of side-chain microphase in polymers was found to significantly enhance the selectivity in hydrocarbon separation processes.
We have synthesized a number of comb-like polysiloxanes with linear, branched, cyclic and silicon-containing substituents; most of them are new and previously not studied polymers. The physicochemical properties of comb-like polysiloxanes have been systematically investigated. Differential-scanning calorimetry and wide-angle X-ray scattering data revealed the side-chain microphase assembly for polymers with linear aliphatic substituents, while the polymers with bulky substituents did not form a microphase. It is shown that the ratio of microphase in the polymer is greater, the closer the values of the thickness of the microphase layer and the length of the cross-link. The effect of the side-chain substituent on the hydrocarbon transport properties of comb-like polysiloxanes was studied. All synthesized polymers are promising as membrane materials for a vital process of hydrocarbon separation. This is associated with an increase in the solubility selectivity of n-butane/methane because the solubility coefficient of methane sharply decreases when long side chains are introduced into the polysiloxane. It was shown for the first time that microphase forming polymers have a significantly higher butane/methane selectivity (23.2-27.5) than polysiloxanes not forming a microphase (selectivity 12.3-20.0). The effect is demonstrated on polysiloxanes with various types of side substituents. It was revealed that for the comb-like polysiloxanes, the diffusivity selectivity and permselectivity are proportional to the fraction of the side-chain microphase in the polymer. With the increase in the hydrocarbon microphase share, the diffusion coefficient of the permanent gas methane is decreasing more rapidly than n-butane, which dissolves well in hydrocarbons and plasticizes polymer. Consequently, the polymers forming the microphase have a higher selectivity C3+/CH4 in the separation of a multicomponent hydrocarbons mixture. (C) 2021 Elsevier Ltd. All rights reserved.
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