Synthetic membrane

Summary

An artificial membrane, or synthetic membrane, is a synthetically created membrane which is usually intended for separation purposes in laboratory or in industry. Synthetic membranes have been successfully used for small and large-scale industrial processes since the middle of twentieth century. A wide variety of synthetic membranes is known. They can be produced from organic materials such as polymers and liquids, as well as inorganic materials. The most of commercially utilized synthetic membranes in separation industry are made of polymeric structures. They can be classified based on their surface chemistry, bulk structure, morphology, and production method. The chemical and physical properties of synthetic membranes and separated particles as well as a choice of driving force define a particular membrane separation process. The most commonly used driving forces of a membrane process in industry are pressure and concentration gradients. The respective membrane process is therefore

Official source

https://en.wikipedia.org/wiki/Synthetic_membrane

About this result

This page is automatically generated and may contain information that is not correct, complete, up-to-date, or relevant to your search query. The same applies to every other page on this website. Please make sure to verify the information with EPFL's official sources.

Related publications (27)

Related publications

Related people

Related units

No results

Related units

Related concepts (12)

Related concepts

Related courses (4)

Related courses

Related lectures (5)

Related lectures

Related publications (27)

Surface modification of PES virus filtration membrane

Claire Roulin

Virus filtration by size exclusion is a robust means of eliminating viruses in blood or pharma products. Porous polymer membranes with a narrow size distribution are used to allow passage of the protein product but retain viruses. The chosen polymer must resist process-induced physical and chemical wear and is therefore generally inert and hydrophobic material. When filtrating potentially heterogeneous products such as IgG from pooled blood samples, protein adsorption on the polymer surface causes high fouling. This eventually blocks the filter and reduces total filtration volume. A solution to this adsorption problem is to graft a hydrophilic gel-like polymer layer on the membrane inner surface to reduce protein adsorption. The surface properties are thus changed while retaining the stability of the bulk polymer. The grafting was initiated with an electron beam, which creates free radicals by unspecific scission of the polymer backbone through electron irradiation. Two acrylate monomers were used for polymerization, a monofunctional monomer and a bifunctional one, used as a crosslinker to form the gel structure. Two different grafting method were tested. The first grafting method is simultaneous grafting, where the membrane is impregnated with the monomer solution then irradiated. Initiation and polymerization thus occur almost simultaneously. The grafted membrane properties were assessed using flow measurements, protein adsorption tests, FTIR absorbance measurements, virus retention tests and filter integrity tests. Comparing the various grafting approaches, it can be seen that simultaneous grafting lowers considerably protein adsorption, to the price of a highly reduced buffer flow. These filters therefore run slowly but can process more volume before fouling. The sequential grafting method using peroxides as initiators did not show significant filtration improvements compared to the reference membrane when the solution with monomer and crosslinker was used. However, when only monofunctional monomer was used for peroxidation grafting, the protein filtration capacity was increased with limited buffer flow loss. Generally, the sequential method is interesting for graft polymerization of porous membranes because it allows higher degree of grafting and the versatile grafting parameters involved give many development options depending on the application

2010

Pretreatment options for micropollutant abatement before aquifer recharge in drinking water production: Assessment of UV/H2O2 and dense membranes

Robin Wünsch

Micropollutants (MP) such as residues of pharmaceuticals, industrial chemicals or pesticides can be detected in almost all water resources. Various processes can be used to abate them in drinking water treatment, e.g., ozonation, advanced oxidation processes (AOP), adsorption on activated carbon or membrane filtration. The selection of a suitable process combination is a complex task for water suppliers.This thesis compares two process chains in the context of a multi-barrier system including managed aquifer recharge (MAR). To protect soils and aquifers from MP in the future, an additional barrier against MP upstream of the MAR was investigated: (1) a full-stream treatment using the AOP UV/H2O2, and (2) a side-stream treatment with low-pressure reverse osmosis (LPRO) or nanofiltration (NF) and ozonation of the retentate to treat the concentrated MPs.Pilot-scale experiments were conducted to determine the relative abatements of MP by UV/H2O2 treatment and by a subsequent soil column treatment. Compared to a soil column fed with water without UV/H2O2 pretreatment, the performance of the combined process (UV/H2O2 + soil column) was more efficient. However, this could be explained by an additive effect of the individual processes.Relative abatements in the UV/H2O2 process are mainly based on the introduced UV fluence and hydroxyl radical exposure. These parameters could be calculated with a model based on the measured relative abatements of two MPs (probe compounds) and their kinetic data (second-order rate constants for the reactions with hydroxyl radical, absorbance and quantum yield).With this information, the relative abatements of other MPs could be predicted with an accuracy of ±20%. A sensitivity analysis of the model showed that the relative abatements of the selected probe compounds should be >50%. In this case, the accuracy of the calculated parameters depends mainly on the precision of the kinetic data.In the case of membrane-based treatment of water by LPRO or NF, a concentrate is produced. Ozonation to treat MP in the concentrate is accompanied by a formation of the possibly carcinogenic bromate by oxidation of bromide. To achieve the highest possible MP abatement with simultaneously low bromate formation, both membrane selection and subsequent concentrate ozonation were investigated. In laboratory tests with standardized concentrates, neither the water source nor the membrane type caused a change in bromate yield for similar relative MP abatements. However, NF membranes have lower relative retentions of bromide and MP than LPRO membranes, making NF concentrates more suitable for ozonation with limited bromate formation.A comparison of UV/H2O2 with membrane treatment showed that full-stream treatment with UV/H2O2 has about four times lower costs and an about five times lower environmental impact. In addition it achieves significantly higher disinfection. In contrast, side-stream treatment with LPRO causes up to two times lower impacts for the environment when the electrical energy source is wind or hydropower. This study thus contributes technical, economic, and environmental aspects to a holistic evaluation of the two process options.

EPFL2022

The coupling of stimuli-responsive macromolecules to nanostructured surfaces opens the perspective for the fabrication and integration of "smart" micro- and nano-electro-mechanical systems (MEMS&NEMS) in which the smallest motile unit is the polymeric chain. The goal of this work was to develop thermoresponsive, durable nanoporous surfaces as a first step toward the fabrication of functional nanocontainers and nanovalves. The proposed strategy involves in a first step the design and implementation of a clean-room compatible, reproducible and up-scalable method for defining organized nanoporous arrays in MEMS compatible surfaces, such as silicon, silicon oxide and silicon nitride. The main objective of the second step was the covalent immobilization of responsive macromolecules on the obtained structures, as to provide the later with a "smart" behavior. The nanostructuring step was realized by block-copolymer assisted lithography. This newly developed technique enables the definition of nanoscale features on semiconductor substrates over large surface areas and in a cost effective manner. A novel method for patterning thin metal films by a lift-off approach, using spin coated block-copolymer micelles monolayers as a template, was investigated. The obtained nanoporous mask was used as resist for the structuring of hard substrates in plasma-assisted processes and structures with aspect ratios as high as 1:10 were be obtained. By using different block-copolymer micelles and spin-coating conditions, the proposed approach enables the variation of the nanopores' diameter from 40 to 80 nm and a surface coverage between 11.7% and 25.5 % in an independent manner. This technique was successfully integrated in a standard microfabrication process for the batch production of thin nanoporous silicon nitride membranes. The 100 nm thick membranes span over thousands of square micrometers and present porosities higher than 109 pores/cm2. They are thus competitive in terms of porosity with the commercially available polymeric membranes. In addition they are two orders of magnitude thinner than polymeric membranes, this making them extremely interesting for applications where permeation rate or response time is important. The rapid flow of water soluble small molecular species through the nanopores was demonstrated in a qualitative manner in this work. Another series of investigations targeted the functionalization of the available nanoporous surfaces with responsive molecules. Poly(N-isopropyl acrylamide) (PNIPAAM) was chosen as a model system. Its coupling to silicon surfaces by a "grafting-to" approach from melt, using an epoxy-functionalized silane as anchoring layer was studied. The analysis of the yielded grafting density showed results superior to those obtained by classic grafting-to approaches. The relation between the polymer's weight and its responsiveness was investigated in liquid media by atomic force microscopy and by dynamic force spectroscopy. Polymers with more than 500 monomers in the back bone were shown to exhibit enhanced responsiveness. Additionally, two bioengineered polymers from the class of elastin-like polymers (ELPs) were investigated as possible candidates for the fabrication of stimuli responsive nanovalves. The molecules were synthesized in collaboration with the Bioforge group (Universidad de Valladolid, Spain) and details of the bioproduction process are presented. A method for the covalent photoattachment of macromolecules using a benzophenone-functionalized silane, was tested in this work. First the capacity of the benzophenone silane to graft synthetic thermo-responsive polymers such as PNIPAAM was demonstrated. The temperature-induced morphology change of the photografted PNIPAAM was not affected by this anchoring strategy and was monitored by tapping AFM in liquid media. The investigations were then extended to the photo-immobilization of ELPs on nanoporous silicon surfaces and the XPS measurements revealed the success of this step. However no conformation modification of the proteins could be evidenced by tapping-mode AFM in liquid media under different ionic strengths.

EPFL2009