2022
DOI: 10.1016/j.memsci.2022.120847
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New sustainable routes for gas separation membranes: The properties of poly(hydroxybutyrate-co-hydroxyvalerate) cast from green solvents

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Cited by 16 publications
(31 citation statements)
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“…Specifically, the band at 2882 cm −1 and peaks in the range of 1300–800 cm −1 are attributed to the CH 2 occurring in the PEG structure (stretching, wagging, twisting, and rocking) [ 30 , 31 ]. Moreover, the signal at 1721 cm −1 , commonly attributed to the carbonyl stretching of the PHB polyester structure [ 32 ], is clearly visible. Nevertheless, no signal that clearly confirms the formation of the bond between the two polymers was detected by FT-IR.…”
Section: Resultsmentioning
confidence: 99%
“…Specifically, the band at 2882 cm −1 and peaks in the range of 1300–800 cm −1 are attributed to the CH 2 occurring in the PEG structure (stretching, wagging, twisting, and rocking) [ 30 , 31 ]. Moreover, the signal at 1721 cm −1 , commonly attributed to the carbonyl stretching of the PHB polyester structure [ 32 ], is clearly visible. Nevertheless, no signal that clearly confirms the formation of the bond between the two polymers was detected by FT-IR.…”
Section: Resultsmentioning
confidence: 99%
“…The thickness was measured to be 19 ± 1 µm. The crystallinity was not provided by the producers and was determined to be equal to 42 ± 1% through DSC analysis, as described in Section S1 of the Supporting Information (SI) [ 19 ]. Gases used for sorption tests, namely methane (CH 4 ) and carbon dioxide (CO 2 ), were purchased from Fluido Tecnica (Campi Bisenzio, FI, Italy) with purities ≥ 99.5%.…”
Section: Methodsmentioning
confidence: 99%
“…The solubility coefficient obtained from the Widom analysis and averaged over three configurations for each system was used to calculate the corresponding number of gas molecules to insert into each system at atmospheric pressure. The calculation was done under the assumption of a quasi-constant solubility coefficient at temperatures higher than the glass transition (T g ) in PHBV, as confirmed by previous experimental work [ 19 ]. After the energy minimization, a short NVT run, a 10 ns NPT run, and a second 1 ns NVT run were performed for equilibration.…”
Section: Methodsmentioning
confidence: 99%
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“…Among DACs, several studies reported the use of commercially available cyclic carbonates, namely, ethylene carbonate (EC), propylene carbonate (PC), and butylene carbonate (BC) as green solvents for membrane preparation, ,, while applications of acyclic DACs in this field is almost unexplored apart from some tests involving dimethyl carbonate (DMC) and diethyl carbonate (DEC). , Although the aforementioned cyclic carbonates are produced industrially at low cost, the lack of diversity across their chemical structures means they can only be used to solubilize a limited number of polymers. Furthermore, in some cases, high temperatures (up to 130 °C) are required to achieve homogeneous polymer solutions. , To overcome these issues, DACs possessing different functional groups could be employed, but this usually means low scale industrial production and a higher market price. , …”
Section: Introductionmentioning
confidence: 99%