Effect of Molecular Structure on the Gas Permeability of Cellulose Aliphatate Esters
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Effect of Molecular Structure on the Gas Permeability of Cellulose Aliphatate Esters
Chinese Journal of Polymer ScienceVol. 32, Issue 1, Pages: 1-8(2014)
Affiliations:
Beijing National Laboratory for Molecular Sciences, CAS Key Laboratory of Engineering Plastics, Institute of Chemistry, Chinese Academy of Sciences, Beijing 100190, China
Jing Chen, Jin-ming Zhang, Ye Feng, et al. Effect of Molecular Structure on the Gas Permeability of Cellulose Aliphatate Esters[J]. Chinese Journal of Polymer Science, 2014, 32(1): 1-8.
DOI:
Jing Chen, Jin-ming Zhang, Ye Feng, et al. Effect of Molecular Structure on the Gas Permeability of Cellulose Aliphatate Esters[J]. Chinese Journal of Polymer Science, 2014, 32(1): 1-8.DOI: 10.1007/s10118-014-1384-2.
Effect of Molecular Structure on the Gas Permeability of Cellulose Aliphatate Esters
cellulose butyrate (CB) and cellulose acetate butyrate (CAB) are synthesized by the homogeneous acylation reactions in cellulose/AmimCl solutions. These cellulose aliphatate esters are used to prepare gas separation membranes and the effects of molecular structure
such as substituent type
degree of substitution (DS) and distribution of substituents
on the gas permeability are studied. For CAs
as the DS increases
their gas permeabilities for all five gases (O
2
N
2
CH
4
CO and CO
2
) increase
and the ideal permselectivity significantly increases first and then slightly decreases. At similar DS value
the homogenously synthesized CA (distribution order of acetate substituent: C6
>
C3
>
C2) is superior to the heterogeneously synthesized CA (distribution order of acetate substituent: C3
>
C2
>
C6) in gas separation. With the increase of chain length of aliphatate substituents from acetate to propionate
and to butyrate
the gas permeability of cellulose aliphatate esters gradually increases. The cellulose mixed ester CAB with short acetate groups and relatively long butyrate groups exhibits higher gas permeability or better permselectivity than individual CA or CB
via
the alteration of the DS of two substituents.
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Related Institution
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