A model for the permeation characteristics of porous membranes with grafted polyelectrolyte brushes

1991 ◽  
Vol 146 (1) ◽  
pp. 251-275 ◽  
Author(s):  
Sanjay Misra ◽  
Sasidhar Varanasi
Keyword(s):  
Porous Membranes ◽  
Polyelectrolyte Brushes

scholarly journals Effects of Amino Acid Side-Chain Length and Chemical Structure on Anionic Polyglutamic and Polyaspartic Acid Cellulose-Based Polyelectrolyte Brushes

Polymers ◽  
2021 ◽  
Vol 13 (11) ◽  
pp. 1789
Author(s):  
Dmitry Tolmachev ◽  
George Mamistvalov ◽  
Natalia Lukasheva ◽  
Sergey Larin ◽  
Mikko Karttunen
Keyword(s):  
Glutamic Acid ◽  
Chain Length ◽  
Chemical Structure ◽  
Side Chain ◽  
Side Chains ◽  
Side Chain Length ◽  
Polyelectrolyte Brushes ◽  
Grafting Density ◽  
The Difference ◽  
Cellulose Surface

We used atomistic molecular dynamics (MD) simulations to study polyelectrolyte brushes based on anionic α,L-glutamic acid and α,L-aspartic acid grafted on cellulose in the presence of divalent CaCl2 salt at different concentrations. The motivation is to search for ways to control properties such as sorption capacity and the structural response of the brush to multivalent salts. For this detailed understanding of the role of side-chain length, the chemical structure and their interplay are required. It was found that in the case of glutamic acid oligomers, the longer side chains facilitate attractive interactions with the cellulose surface, which forces the grafted chains to lie down on the surface. The additional methylene group in the side chain enables side-chain rotation, enhancing this effect. On the other hand, the shorter and more restricted side chains of aspartic acid oligomers prevent attractive interactions to a large degree and push the grafted chains away from the surface. The difference in side-chain length also leads to differences in other properties of the brush in divalent salt solutions. At a low grafting density, the longer side chains of glutamic acid allow the adsorbed cations to be spatially distributed inside the brush resulting in a charge inversion. With an increase in grafting density, the difference in the total charge of the aspartic and glutamine brushes disappears, but new structural features appear. The longer sides allow for ion bridging between the grafted chains and the cellulose surface without a significant change in main-chain conformation. This leads to the brush structure being less sensitive to changes in salt concentration.

Low-Concentration Salt Solution Changes the Interfacial Molecular Behavior of Polyelectrolyte Brushes

2021 ◽  
Author(s):  
Yongsheng Luo ◽  
Chu Wang ◽  
Ai-Ping Pang ◽  
Xiang Zhang ◽  
Dayang Wang ◽  
...  
Keyword(s):  
Salt Solution ◽  
Low Concentration ◽  
Polyelectrolyte Brushes ◽  
Molecular Behavior ◽  
Solution Changes

scholarly journals Towards explicit regulating-ion-transport: nanochannels with only function-elements at outer-surface

2021 ◽  
Vol 12 (1) ◽  
Author(s):  
Qun Ma ◽  
Yu Li ◽  
Rongsheng Wang ◽  
Hongquan Xu ◽  
Qiujiao Du ◽  
...  
Keyword(s):  
Ion Transport ◽  
Numerical Simulations ◽  
Power Density ◽  
Outer Surface ◽  
Internal Resistance ◽  
Porous Membranes ◽  
Two Dimensional ◽  
Ionic Selectivity ◽  
Key Features ◽  
Energy Conversion Devices

AbstractFunction elements (FE) are vital components of nanochannel-systems for artificially regulating ion transport. Conventionally, the FE at inner wall (FEIW) of nanochannel−systems are of concern owing to their recognized effect on the compression of ionic passageways. However, their properties are inexplicit or generally presumed from the properties of the FE at outer surface (FEOS), which will bring potential errors. Here, we show that the FEOS independently regulate ion transport in a nanochannel−system without FEIW. The numerical simulations, assigned the measured parameters of FEOS to the Poisson and Nernst-Planck (PNP) equations, are well fitted with the experiments, indicating the generally explicit regulating-ion-transport accomplished by FEOS without FEIW. Meanwhile, the FEOS fulfill the key features of the pervious nanochannel systems on regulating-ion-transport in osmotic energy conversion devices and biosensors, and show advantages to (1) promote power density through concentrating FE at outer surface, bringing increase of ionic selectivity but no obvious change in internal resistance; (2) accommodate probes or targets with size beyond the diameter of nanochannels. Nanochannel-systems with only FEOS of explicit properties provide a quantitative platform for studying substrate transport phenomena through nanoconfined space, including nanopores, nanochannels, nanopipettes, porous membranes and two-dimensional channels.

scholarly journals Determination of the molar mass of surface-grafted weak polyelectrolyte brushes using force spectroscopy

Polymer ◽  
2015 ◽  
Vol 67 ◽  
pp. 111-117 ◽  
Author(s):  
Ateyyah AL-Baradi ◽  
Michael R. Tomlinson ◽  
Zhenyu J. Zhang ◽  
Mark Geoghegan
Keyword(s):  
Molar Mass ◽  
Force Spectroscopy ◽  
Polyelectrolyte Brushes

scholarly journals Effect of moisture condensation on vapour transmission through porous membranes

2021 ◽  
pp. 152808372110142
Author(s):  
Ariana Khakpour ◽  
Michael Gibbons ◽  
Sanjeev Chandra
Keyword(s):  
Water Vapour ◽  
Moisture Diffusion ◽  
Porous Membrane ◽  
Water Evaporation ◽  
Porous Membranes ◽  
Water Vapour Concentration ◽  
Vapour Concentration ◽  
Vapour Diffusion ◽  
Pore Blockage ◽  
The Impact

Porous membranes find natural application in various fields and industries. Water condensation on membranes can block pores, reduce vapour transmissibility, and diminish the porous membranes' performance. This research investigates the rate of water vapour transmission through microporous nylon and nanofibrous Gore-Tex membranes. Testing consisted of placing the membrane at the intersection of two chambers with varied initial humidity conditions. One compartment is initially set to a high ([Formula: see text]water vapour concentration and the other low ([Formula: see text], with changes in humidity recorded as a function of time. The impact of pore blockage was explored by pre-wetting the membranes with water or interposing glycerine onto the membrane pores before testing. Pore blockage was measured using image analysis for the nylon membrane. The mass flow rate of water vapour ( ṁv) diffusing through a porous membrane is proportional to both its area (A) and the difference in vapour concentration across its two faces ([Formula: see text], such that [Formula: see text] where K is defined as the moisture diffusion coefficient. Correlations are presented for the variation of K as a function of [Formula: see text]. Liquid contamination on the porous membrane has been shown to reduce the moisture diffusion rate through the membrane due to pore blockage and the subsequent reduced open area available for vapour diffusion. Water evaporation from the membrane's surface was observed to add to the mass of vapour diffusing through the membrane. A model was developed to predict the effect of membrane wetting on vapour diffusion and showed good agreement with experimental data.

Charged microgels adsorbed on porous membranes - A study of their mobility and molecular retention

2019 ◽  
Vol 588 ◽  
pp. 117190 ◽  
Author(s):  
Monika Wiese ◽  
Theresa Lohaus ◽  
Jan Haussmann ◽  
Matthias Wessling
Keyword(s):  
Porous Membranes
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