2018
DOI: 10.1021/acsami.8b11657
|View full text |Cite
|
Sign up to set email alerts
|

Selective Adsorption and Separation of Xylene Isomers and Benzene/Cyclohexane with Microporous Organic Polymers POP-1

Abstract: The separation of chemical substances with analogous chemical structures and physical properties remains a great challenge. In this work, triptycene-like microporous organic polymers (MOPs), POP-1, was synthesized via choosing 1,4-dimethoxybenzene (DMB) and triptycene as external cross-linkers and building blocks, respectively, and POP-1 was employed to separate xylene isomers and benzene (Bz)/cyclohexane (Cy). Results show that POP-1 has a higher uptake for m-xylene (0.29 g/g) and Bz (1.02 g/g); more intrigui… Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
2
2
1

Citation Types

1
38
0

Year Published

2019
2019
2024
2024

Publication Types

Select...
8

Relationship

0
8

Authors

Journals

citations
Cited by 58 publications
(39 citation statements)
references
References 55 publications
(84 reference statements)
1
38
0
Order By: Relevance
“…The triptycene‐like microporous organic polymer POP‐1 was reported for the separation of xylene isomers. [109c] The weak CH/π interactions were successfully used to tune the host–guest interactions and to achieve separation of xylene isomers. In 2019, COFs were first reported by Huang and co‐workers for the separation of xylene isomers and ethylbenzene.…”
Section: Separation Of C 8 Aromaticsmentioning
confidence: 99%
“…The triptycene‐like microporous organic polymer POP‐1 was reported for the separation of xylene isomers. [109c] The weak CH/π interactions were successfully used to tune the host–guest interactions and to achieve separation of xylene isomers. In 2019, COFs were first reported by Huang and co‐workers for the separation of xylene isomers and ethylbenzene.…”
Section: Separation Of C 8 Aromaticsmentioning
confidence: 99%
“…3c) were described. The binding energy between biurea and DEC was evaluated, and the resulting binding energy of −33.05 kJ mol −1 was within the range of conventional hydrogen bonds [37]. The distances from the H atom of the imino and amino groups of biurea to the O atom of the carbonyl group of DEC are 2.43 and 2.15 Å in the optimized adduct, respectively.…”
Section: Resultsmentioning
confidence: 85%
“…These results evidently hint that the PSD of TBPALs may be tuned easily by changing the number of reactive sites in the monomers. The microporosity present in TBPALs is ascribed to the incorporation of the rigid 3D triptycene units in the polymer network (Chen et al, 2016;Roy et al, 2017;Bera et al, 2018bBera et al, , 2019Tan et al, 2018).…”
Section: Resultsmentioning
confidence: 99%