Influence of cross-linking and process parameters on the separation performance of poly(dimethylsiloxane) nanofiltration membranes

被引:46
作者
Robinson, JP
Tarleton, ES [1 ]
Ebert, K
Millington, CR
Nijmeijer, A
机构
[1] Loughborough Univ Technol, Dept Chem Engn, Adv Separat Technol Grp, Loughborough LE11 3TU, Leics, England
[2] GKSS Forschungszentrum Geesthacht GmbH, Inst Chem, D-21502 Geesthacht, Germany
[3] Shell Res Ltd, Global Solut, Chester CH1 3SH, Cheshire, England
[4] Shell Global Solut Int BV, NL-1030 BN Amsterdam, Netherlands
关键词
D O I
10.1021/ie0496277
中图分类号
TQ [化学工业];
学科分类号
0817 ;
摘要
The separation of organic solutes in organic solvents was assessed using dense poly(dimethyl-siloxane) (PDMS) membranes with different degrees of cross-linking and varying thickness of the dense PDMS layer. The predominant rejection mechanism for low-polarity organic solutes is shown to occur via size exclusion, with the rejection also being dependent on the degree of membrane cross-linking, the swelling propensity of the membrane-feed stream, and the transmembrane pressure. It is postulated that the size-exclusion mechanism arises as a consequence of the relatively large degree of swelling of the PDMS material (up to 300%), which induces appreciable regions between the polymer chains for solvent and solute transport to take place. The degree of swelling governs the relative size of the transport regions within the membrane and, hence, the overall solvent flux and solute rejection characteristics. It is shown that solvent-solute coupling plays a major role in solute transport, with the convective element of solute flow increasing as the degree of swelling increases and the solute size decreases. Despite the existence of a size-exclusion mechanism, it is difficult to rule out the solution-diffusion model as an interpretation of the data; however, it is also demonstrated that models based on pore flow can adequately define the experimental data. The similarities between the two approaches are discussed, and potential evidence of a transition between solution diffusion and pore flow is introduced.
引用
收藏
页码:3238 / 3248
页数:11
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