Enhanced Accumulation of Colloidal Particles in Microgrooved Channels via Diffusiophoresis and Steady-State Electrolyte Flows.
Enhanced Accumulation of Colloidal Particles in Microgrooved Channels via Diffusiophoresis and Steady-State Electrolyte Flows.
复制标题
DOI:
10.1021/acs.langmuir.2c01755
复制
发表时间:
2022-11-22
期刊:
影响因子:
3.9
通讯作者:
Bolognesi, Guido
中科院分区:
文献类型:
--
作者:
Singh, Naval;Vladisavljevic, Goran T.;Nadal, Francois;Cottin-Bizonne, Cecile;Pirat, Christophe;Bolognesi, Guido
The delivery of colloidal particles in dead-end microstructures is very challenging, since these geometries do not allow net flows of particle-laden fluids; meanwhile, diffusive transport is slow and inefficient. Recently, we introduced a novel particle manipulation strategy, based on diffusiophoresis, whereby the salt concentration gradient between parallel electrolyte streams in a microgrooved channel induces the rapid (i.e., within minutes) and reversible accumulation, retention, and removal of colloidal particles in the microgrooves. In this study, we investigated the effects of salt contrast and groove depth on the accumulation process in silicon microgrooves and determined the experimental conditions that lead to a particle concentration peak of more than four times the concentration in the channel bulk. Also, we achieved an average particle concentration in the grooves of more than twice the concentration in the flowing streams and almost 2 orders of magnitude larger than the average concentration in the grooves in the absence of a salt concentration gradient. Analytical sufficient and necessary conditions for particle accumulation are also derived. Finally, we successfully tested the accumulation process in polydimethylsiloxane microgrooved channels, as they are less expensive to fabricate than silicon microgrooved substrates. The controlled and enhanced accumulation of colloidal particles in dead-end structures by solute concentration gradients has potential applications in soft matter and living systems, such as drug delivery, synthetic biology, and on-chip diagnostics.
登录
查看更多内容
影响因子:
3.4
作者:
Huff M
通讯作者:
Huff M
影响因子:
16.6
作者:
Friedrich SM;Burke JM;Liu KJ;Ivory CF;Wang TH
通讯作者:
Wang TH
影响因子:
16.6
作者:
Bolognesi G;Friddin MS;Salehi-Reyhani A;Barlow NE;Brooks NJ;Ces O;Elani Y
通讯作者:
Elani Y
影响因子:
17.1
作者:
Kar, Abhishek;Chiang, Tso-Yi;Velegol, Darrell
通讯作者:
Velegol, Darrell
影响因子:
41.2
作者:
Abecassis, B.;Cottin-Bizonne, C.;Bocquet, L.
通讯作者:
Bocquet, L.