Browse
Submit Data
Databases
API
Help

Dataset Information

22 Views

0 Connections

0 Citations

0 Reanalyses

0 Downloads

Omics score: 0

Alleviation of Reverse Salt Leakage across Nanofiber Supported Thin-Film Composite Forward Osmosis Membrane via Heat-Curing in Hot Water.

ABSTRACT: Electrospun nanofiber with interconnected porous structure has been studied as a promising support layer of polyamide (PA) thin-film composite (TFC) forward osmosis (FO) membrane. However, its rough surface with irregular pores is prone to the formation of a defective PA active layer after interfacial polymerization, which shows high reverse salt leakage in FO desalination. Heat-curing is beneficial for crosslinking and stabilization of the PA layer. In this work, a nanofiber-supported PA TFC membrane was conceived to be cured on a hot water surface with preserved phase interface for potential "defect repair", which could be realized by supplementary interfacial polymerization of residual monomers during heat-curing. The resultant hot-water-curing FO membrane with a more uniform superhydrophilic and highly crosslinked PA layer exhibited much lower reverse salt flux (FO: 0.3 gMH, PRO: 0.8 gMH) than that of oven-curing FO membrane (FO: 2.3 gMH, PRO: 2.2 gMH) and achieved ∼4 times higher separation efficiency. It showed superior stability owing to mitigated reverse salt leakage and osmotic pressure loss, with its water flux decline lower than a quarter that of the oven-curing membrane. This study could provide new insight into the fine-tuning of nanofiber-supported TFC FO membrane for high-quality desalination via a proper selection of heat-curing methods.

SUBMITTER: Ke XX

PROVIDER: S-EPMC8066147 | biostudies-literature |

REPOSITORIES: biostudies-literature

ACCESS DATA

Json Xml

Similar Datasets

Thin Film Biocomposite Membrane for Forward Osmosis Supported by Eggshell Membrane.

Project description:There is a general drive to adopt highly porous and less tortuous supports for forward osmosis (FO) membranes to reduce internal concentration polarization (ICP), which regulates the osmotic water permeation. As an abundant waste material, eggshell membrane (ESM) has a highly porous and fibrous structure that meets the requirements for FO membrane substrates. In this study, a polyamide-based biocomposite FO membrane was fabricated by exploiting ESM as a membrane support. The polyamide layer was deposited by the interfacial polymerization technique and the composite membrane exhibited osmotically driven water flux. Further, biocomposite FO membranes were developed by surface coating with GO for stable formation of the polyamide layer. Finally, the osmotic water flux of the eggshell composite membrane with a low structural parameter (~138 µm) reached 46.19 L m-2 h-1 in FO mode using 2 M NaCl draw solution.

| S-EPMC8879599 | biostudies-literature

Impact of Graphene Oxide on Properties and Structure of Thin-Film Composite Forward Osmosis Membranes.

Project description:Forward osmosis (FO) membranes have the advantages of low energy consumption, high water recovery rate, and low membrane pollution trend, and they have been widely studied in many fields. However, the internal concentration polarization (ICP) caused by the accumulation of solutes in the porous support layer will reduce permeation efficiency, which is currently unavoidable. In this paper, we doped Graphene oxide (GO) nanoparticles (50~150 nm) to a polyamide (PA) active layer and/or polysulfone (PSF) support layer, investigating the influence of GO on the morphology and properties of thin-film composite forward osmosis (TFC-FO) membranes. The results show that under the optimal doping amount, doping GO to the PA active layer and PSF support layer, respectively, is conducive to the formation of dense and uniform nano-scale water channels perpendicular to the membrane surface possessing a high salt rejection rate and low reverse solute flux without sacrificing high water flux. Moreover, the water channels formed by doping GO to the active layer possess preferable properties, which significantly improves the salt rejection and water permeability of the membrane, with a salt rejection rate higher than 99% and a water flux of 54.85 L·m-2·h-1 while the pure PSF-PA membrane water flux is 12.94 L·m-2·h-1. GO-doping modification is promising for improving the performance and structure of TFC-FO membranes.

| S-EPMC9506024 | biostudies-literature

Molecularly tunable thin-film nanocomposite membranes with enhanced molecular sieving for organic solvent forward osmosis.

Project description:Thin-film nanocomposites (TFN) functionalized with tunable molecular-sieving nanomaterials have been employed to tailor membranes, with an enhanced permeability and selectivity. Herein, water-soluble hollow cup-like macrocyclic molecules, sulfothiacalix[4]arene (STCAss) and sulfocalix[4]arene (SCA), are ionically bonded into the polyamide network to engineer the molecular-sieving properties of TFN membranes for organic solvent forward osmosis (OSFO). Introducing both STCAss and SCA into the polyamide network not only increases the free volume, but also reduces the thickness of the TFN layers. Combining with their molecularly tunable size of the lower cavities, both STCAss and SCA enable the TFN membranes to size exclusively reject the draw solutes, but only STCAss-functionalized membrane has an ethanol flux doubling the pristine one under the FO and PRO modes in OSFO processes; leading the functionalized polyamide network with remarkable improvements in OSFO performance. This study may provide insights to molecularly functionalize TFN membranes using multifunctional nano-fillers for sustainable separations.

| S-EPMC7057969 | biostudies-literature

Thin Film Composite Forward Osmosis Membrane with Single-Walled Carbon Nanotubes Interlayer for Alleviating Internal Concentration Polarization.

Project description:This study reported a series of thin film composite (TFC) membranes with single-walled nanotubes (SWCNTs) interlayers for the forward osmosis (FO) application. Pure SWCNTs with ultrahigh length-to-diameter ratio and without any functional group were applied to form an interconnect network interlayer via strong ?-? interactions. Compared to the TFC membrane without SWCNTs interlayer, our TFC membrane with optimal SWCNTs interlayer exhibited more than three times the water permeability (A) of 3.3 L m-2h-1bar-1 in RO mode with 500 mg L-1 NaCl as feed solution and nearly three-fold higher FO water flux of 62.8 L m-2 h-1 in FO mode with the deionized water as feed solution and 1 M NaCl as draw solution. Meanwhile, the TFC membrane with SWCNTs interlayer exhibited significantly reduced membrane structure parameters (S) to immensely mitigate the effect of internal concentration polarization (ICP) in support layer with micro-sized pores in favor of higher water flux. It showed that the pure SWCNTs interlayer could be an effective strategy to apply in FO membranes.

| S-EPMC7077303 | biostudies-literature

Novel Polysulfone/Carbon Nanotube-Polyamide Thin Film Nanocomposite Membranes with Improved Water Flux for Forward Osmosis Desalination.

Project description:Forward osmosis (FO) is a promising alternative to reverse osmosis (RO) in membrane-based water desalination. In the current study, carboxylated multiwalled carbon nanotubes (MWCNTs) were incorporated in a polyamide (PA) layer formed on top of a polysulfone porous support, resulting in a thin film nanocomposite (TFN) membrane. The amount of MWCNTs was varied (0.01, 0.05, 0.1, and 0.2 wt/vol %). The FO performance was investigated using deionized water as the feed solution and 2 M NaCl as the draw solution. It was found that the carboxylated MWCNTs enhanced the membrane hydrophilicity, surface roughness, and porosity. Such combined effects are believed to have led to enhanced FO water flux. TFN 0.2 showed the highest FO water flux of 73.15 L/m2 h, an improvement of 67% compared to the blank thin-film composite (TFC) membrane and significantly better than the values reported in the literature. Direct observation by transmission electron microscopy revealed the presence of some open-ended CNTs favorably oriented across the PA layer. Those are believed to have facilitated the transport of water through their inner cores and contributed to the increase in water flux. However, this was at the expense of salt rejection and reverse solute flux performance. The best performing membrane was found to be TFN 0.01. It exhibited a salt rejection of 90.1% with a FO water flux of 50.23 L/m2 h, which is 13% higher than the TFC membrane, and a reverse solute flux of 2.76 g/m2 h, which is 21% lower than the TFC membrane. This TFN 0.01 membrane also outperformed the TFN membranes reported in the literature.

| S-EPMC7315434 | biostudies-literature

Improved Forward Osmosis Performance of Thin Film Composite Membranes with Graphene Quantum Dots Derived from Eucalyptus Tree Leaves.

Project description:The major challenges in forward osmosis (FO) are low water flux, high specific reverse solute flux (SRSF), and membrane fouling. The present work addresses these problems by the incorporation of graphene quantum dots (GQDs) in the polyamide (PA) layer of thin-film composite (TFC) membranes, as well as by using an innovative polyethersulfone nanofiber support for the TFC membrane. The GQDs were prepared from eucalyptus leaves using a facile hydrothermal method that requires only deionized water, without the need for any organic solvents or reducing agents. The nanofiber support of the TFC membranes was prepared using solution blow spinning (SBS). The polyamide layer with GQDs was deposited on top of the nanofiber support through interfacial polymerization. This is the first study that reports the fouling resistance of the SBS-nanofiber-supported TFC membranes. The effect of various GQD loadings on the TFC FO membrane performance, its long-term FO testing, cleaning efficiency, and organic fouling resistance were analyzed. It was noted that the FO separation performance of the TFC membranes was improved with the incorporation of 0.05 wt.% GQDs. This study confirmed that the newly developed thin-film nanocomposite membranes demonstrated increased water flux and salt rejection, reduced SRSF, and good antifouling performance in the FO process.

| S-EPMC9565292 | biostudies-literature

Novel Thin Film Nanocomposite Forward Osmosis Membranes Prepared by Organic Phase Controlled Interfacial Polymerization with Functional Multi-Walled Carbon Nanotubes.

Project description:Novel high-quality thin film nanocomposite (TFN) membranes for enhanced forward osmosis (FO) were first synthesized through organic phase controlled interfacial polymerization by utilizing functional multi-walled carbon nanotubes (MWCNTs). As 3-aminopropyltriethoxysilane (APTES) grafted MWCNTs via an amidation reaction significantly promoted the dispersion in organic solution, MWCNTs-APTES with better compatibility effectively restricted the penetration of trimesoyl chloride (TMC), thus adjusting the morphology and characters of TFN membranes. Various techniques such as Fourier transform infrared spectra (FTIR), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), scanning electron microscope (SEM), sessile droplet analysis and FO experiments and reverse osmosis (RO) operation were taken to characterize and evaluate the performance of nanocomposites and membranes. The prepared TFN FO membranes exhibited good hydrophilicity and separation efficiency, in which water flux was about twice those of thin film composite (TFC) membranes without MWCNTs-APTES in both AL-DS and AL-FS modes. Compared with the original TFC membrane, the membrane structural parameter of the novel TFN FO membrane sharply was cut down to 60.7%. Based on the large number of low mass-transfer resistance channels provided by functional nanocomposites, the progresses may provide a facile approach to fabricate novel TFN FO membranes with advanced selectivity and permeability.

| S-EPMC8304348 | biostudies-literature

Fabricating robust thin film composite membranes reinforced on woven mesh backing fabric support for pressure assisted and forward osmosis: A dataset.

Project description:The data presented in this paper are produced as part of the original research article entitled "Thin-film composite membrane on a compacted woven backing fabric for pressure assisted osmosis" (Sahebi et al., 2017). This article describes how to fabricate a defect free membrane for forward osmosis (FO) and pressure assisted osmosis (PAO) on the woven mesh backing fabric support. Casting polymer on backing fabric support may limit the interfacial polyemirization due to wrinkled membrane surface. This paper presents data obtained from two different backing fabrics used as support for fabrication of thin film composite FO membrane. Backing fabric support were woven polyester mesh with different opening size. The data include the characterization of the intrinsic properties of the membrane samples, SEM and their performance under FO process. The structural parameters (S value) of the substrate were computed from thickness and porosity of the substrates. Thin film composite (TFC) membrane achieved a water flux of 8.1?L?m2 h-1 in FO process and 37?L?m2 h-1 using 0.5?M NaCl as draw solution (DS) and deionised (DI) water as the feed solution (FS) when applied hydraulic pressure was 10?bar.

| S-EPMC6197614 | biostudies-literature

Thin Film Composite Polyamide Reverse Osmosis Membrane Technology towards a Circular Economy.

Project description:It is estimated that Reverse Osmosis (RO) desalination will produce, by 2025, more than 2,000,000 end-of-life membranes annually worldwide. This review examines the implementation of circular economy principles in RO technology through a comprehensive analysis of the RO membrane life cycle (manufacturing, usage, and end-of-life management). Future RO design should incorporate a biobased composition (biopolymers, recycled materials, and green solvents), improve the durability of the membranes (fouling and chlorine resistance), and facilitate the recyclability of the modules. Moreover, proper membrane maintenance at the usage phase, attained through the implementation of feed pre-treatment, early fouling detection, and membrane cleaning methods can help extend the service time of RO elements. Currently, end-of-life membranes are dumped in landfills, which is contrary to the waste hierarchy. This review analyses up to now developed alternative valorisation routes of end-of-life RO membranes, including reuse, direct and indirect recycling, and energy recovery, placing a special focus on emerging indirect recycling strategies. Lastly, Life Cycle Assessment is presented as a holistic methodology to evaluate the environmental and economic burdens of membrane recycling strategies. According to the European Commission's objectives set through the Green Deal, future perspectives indicate that end-of-life membrane valorisation strategies will keep gaining increasing interest in the upcoming years.

| S-EPMC9502371 | biostudies-literature

New insights into the organic fouling mechanism of an <i>in situ</i> Ca<sup>2+</sup> modified thin film composite forward osmosis membrane.

Project description:In this study, the effect of organic substances on the fouling behavior of a thin film composite (TFC) membrane with in situ Ca2+ addition (TFC-Ca membrane) was evaluated. Bovine serum albumin (BSA), humic acid (HA) and sodium alginate (SA) were used as surrogate foulants for protein, natural organic substances and polysaccharides, respectively, thus enabling the analysis of foulant-membrane interaction in the membrane fouling process. Fouling experiments were carried out and the fouling mechanism was investigated by extended Derjaguin-Landau-Verwey-Overbeek (XDLVO) theory. SEM-EDX, ICP-OES and TOC analysis were applied to characterize the fouled TFC-Ca membrane. Results suggested that the interfacial free energies obtained from advanced contact angle measurements were correlated strongly with the rates of membrane fouling. In situ Ca2+ addition in the TFC membrane resulted in the decrease of the interfacial adhesion free energy (i.e., foulant-membrane interaction) and thus the mitigation of membrane fouling. The permeate flux of TFC-Ca FO membrane after organic fouling could be fully restored by simple physical cleaning. The antifouling mechanism of Ca2+ pre-binding carboxyl groups in the TFC-Ca FO membrane was demonstrated, which provides new insights into the development of antifouling TFC membranes in the future.

| S-EPMC9075835 | biostudies-literature

OmicsDI is part of the ELIXIR infrastructure

OmicsDI is an Elixir interoperability service. Learn more ›

Tweets

OmicsDI Databases

PRIDE
PeptideAtlas
MassIVE
JPOST Repository
Physiome Model Repository

EGA
EVA
ENA
LINCS
PAXDB
Cell Collective

MetaboLights
Metabolomics Workbench
MetabolomeExpress
GNPS
BioModels
FAIRDOMHub

ArrayExpress
dbGaP
ExpressionAtlas
GEO
NODE

Information

Databases
Help
API
Contact us
Code on GitHub
Terms of use
Submit Data