Antifouling Performance Research Articles

Enhancing silica scaling resistance of high-pressure reverse osmosis membranes through surface grafting with various sulfonic acid monomers

Silica scaling is a major challenge in the application of high-pressure reverse osmosis (RO) membranes. In this work, we modified commercially available RO membranes by grafting different sulfonic acid monomers onto their surface using redox polymerization. We systematically studied the effects of various sulfonic acid monomers on membrane performance. Due to the different grafting abilities of sulfonic acid monomers on the membrane, the modified membranes exhibited different physicochemical properties. Simulated silica scaling experiments revealed that the initial permeate flux and sulfonic acid grafting rate of the membrane played crucial roles in its antifouling performance. Molecular dynamics (MD) simulation indicated that the adsorption of silica scale on the membrane was positively correlated with the grafting degree of sulfonic acid monomers. The membrane modified with 3-sulfopropyl potassium methacrylate (SPM) demonstrated a 14 % higher initial flux than the pristine membrane and the highest sulfonic acid grafting rate, resulting in the lowest flux decay rate. Additionally, the SPM modified membrane outperformed the pristine membrane against composite foulants with organic matters and silica. Our research demonstrated that the redox grafting polymerization of sulfonic acid monomers can simultaneously improve the flux and silica scaling resistance of RO membranes without compromising salt rejection. This provides a scalable strategy for preparing RO membranes with enhanced resistance to silica scaling.

Advanced photocatalytic membrane GO-NiFe@SiO2/PVDF for efficient decontamination of synthetic dyes in batik wastewater with superior antifouling features

A novel composite membrane, GO-NiFe@SiO2/polyvinylidene fluoride (PVDF), was prepared via the sol-gel method for nanocomposite synthesis and phase inversion method for membrane fabrication. The investigation encompassed the structural features and properties of the nanocomposite membranes, including photocatalytic activity under UV type C, antifouling capability, and self-cleaning behavior. The degradation of dyes in real Batik wastewater followed pseudo-first-order kinetics, with the GO-NiFe@SiO2/PVDF 1 wt% nanocomposite membranes exhibiting a highest dyes removal efficiency up to 90.50 % within 8 h, compared to the pristine PVDF membrane (60.95 %). The XRD pattern analysis indicates that the incorporation of GO-NiFe@SiO2 into the PVDF membrane induced a transformation in the semi-crystalline phase of PVDF, shifting from the alpha-phase to the beta-phase, consequently facilitating the development of electrostatic charge on the membrane surface. The pore-size distribution analysis revealed that all prepared membranes fall within the range of nanofiltration and tight ultrafiltration (NF-TUF). Additionally, the photocatalytic membrane demonstrated enhanced permeation flux of 30.46 L.m−2.h−1 and flux recovery rate up to 92.57 % under simulated UV light irradiation, showcasing improved antifouling capability. Moreover, the membrane exhibited outstanding cycle test with 6 consecutive cleaning every 3 h, self-cleaning efficiency, with 61.32 % cleaning efficiency under UV irradiation. The incorporation of GO-NiFe@SiO2 enhanced the physicochemical properties of the photocatalytic membrane, including hydrophilicity, surface topologies, and mechanical strength, thereby improving photocatalytic anti-fouling performance and expanding the potential applications of membrane filtration technology.

Efficient removal of per- and polyfluoroalkyl substances by a metal-organic framework membrane with high selectivity and stability

Per- and polyfluoroalkyl substances (PFAS) in water requires sufficient removal due to their extreme chemical stability and potential health risk. Membrane separation can be a promising strategy, while membranes with conventional structures used for PFAS removal often face challenges such as limited efficiency and stability. In this study, a novel metal-organic framework (MOF) membrane with local modification of polyamide (PA) was developed by introducing interfacial polymerization process during the construction of lamellar membranes with MOF nanosheets. Benefiting from the dense structure and strong negative surface charge, the PA-modified MOF membrane could effectively remove 11 types of PFAS (five short-chain and six long-chain ones with molecular weights ranging from 214.0 to 514.1 Da), especially displaying high rejections for short-chain PFAS (over 84%), along with a remarkable water permeance of 21.4 L·m⁻²·h⁻¹·bar⁻1. The membrane removal characteristics for PFAS were deeply analyzed by elucidating various rejection mechanisms, with particularly distinguishing the rejection and adsorption capacity. Moreover, the membrane stability was significantly enhanced, demonstrated by the structural integrity after 10 min of ultrasonic treatment and stable separation efficiency over 120 h of continuous filtration. With enhanced surface hydrophilicity and negative charge as well as dense membrane pores, the novel membrane also exhibited more superior anti-fouling performance compared to conventional lamellar and PA membranes, further manifesting advantages for practical applications. This work provides a promising solution for developing high-performance membranes tailored specifically for efficient PFAS removal, addressing a critical need in water treatment.

Reagent-free anti-fouling electrochemical immunosensor based on AL-BSA/AuNPs/PANI coating for the point-of-care detection of C-reactive protein in plasma and whole blood

Developing the portable CRP detection technologies that are suitable for point-of-care (POC) and primary care management is of utmost importance, and advancing the electrochemical immunosensors hold promise for POC implementation. Nevertheless, non-specific adsorption of numerous interfering proteins in complex biological media contaminates immunosensors, thereby restricting the reliability in detection efficacy. In this study, a three-dimensional flower-leaf shape amyloid bovine serum albumin/gold nanoparticles/polyaniline (AL-BSA/AuNPs/PANI) coating on the surface of the electrode was developed, which demonstrated strong anti-adsorption properties against bovine serum albumin, plasma, and cells. The immunosensor exhibited a good linear relationship to CRP response, featuring a detection limit of 0.09 μg/mL, consistent with clinical reference range. In addition, the CRP immunosensor demonstrated excellent specificity in other inflammation-related proteins and commendable anti-interference performance for CRP detection in plasma and whole blood tests. Importantly, by combining the development of a USB flash disk-type portable electrochemical workstation with a reagent-free mode, the developed CRP electrochemical immunosensor delivered ideal results in clinical samples. The anti-fouling performance, sensitivity and specificity of the immunosensor, as well as its flexible test modes in clinical samples, provide important scientific basis for developing POC detection technologies of vital biomarkers in complex biological media.

Dual defense against membrane fouling for efficient and sustainable oil/water separation on a novel super-hydrophilic/underwater superoleophobic and catalytic nanofibrous membrane

Membrane separation technology is widely recognized as an efficient method for treating organically polluted wastewater in virtue of high performance and straightforward operation. However, the practical application of membranes is inevitably confronted with contamination issues, presenting a major challenge in terms of fouling resistance. To address this issue, a defensive-offensive dual-defense strategy based on wettability and catalytic ability control is proposed. With this concept, a novel nanofibrous membrane with a unique structure was successfully prepared through polyacrylonitrile (PAN) electrospinning, pre-oxidation, CoFe Prussian blue analogue (PBA) and polypyrrole (PPy) modification, and calcination processes. For the passive defense mode, the as-prepared membrane has shown good underwater-superoleophobicity for various types of oils, good separation capability for corresponding oil–water emulsions with retention ratios of above 99 % and fluxes ranging from 231.5 to 1524.2 L·m−2·h−1·bar−1, as well as organic solvent (dimethylformamide, DMF) resistance. For the offensive defense mode, this membrane exhibits well catalytic degradation performance for refractory pollutants with the assistance of peroxymonosulfate (PMS), which is due to the membrane being decorated with catalytic nanoparticles that contain abundant encapsulated ultra-small Fe doped Co3O4 (∼2.28 nm), and that is much smaller than the size of the pristine PBA (∼33.8 nm). Notably, the surfactants present in oil-in-water emulsions are found to be the main cause of membrane fouling, where the cationic surfactants exhibit the most significant fouling effect, while the introduction of photo-Fenton-like catalysis can endow the membrane with excellent antifouling performance and extended service life, and nearly a fully recover of emulsion separation performance was achieved. Overall, this work paves pathways to the design of advanced membranes for sustainable wastewater treatment.

A self-healing polyurethane/imidazole-modified carboxylated graphene oxide composite coating for antifouling and anticorrosion applications

Marine corrosion and biofouling present significant challenges to maintaining maritime vessels and oceanic infrastructure. Developing coatings that integrate anti-fouling, anti-corrosion, and self-healing properties remains a critical issue. This study introduces imidazolium-modified carboxylated graphene (FCGO) into polyurethane coatings (F-PUSS) containing disulfide bonds to address this challenge. The incorporation of FCGO significantly enhances the mechanical properties of the coating, improving tensile stress by 40 % to 20.97 MPa. The barrier properties of FCGO also provide strong corrosion resistance, with |Z|0.01Hz values an order of magnitude higher than the original samples, even after 15 days of immersion in sodium chloride (3.5 wt%). Additionally, F-PUSS retains corrosion resistance after repairs. The synergistic action of imidazole groups and graphene provides excellent antifouling performance with nearly to an alga rate of 100 % and an antimicrobial rate of 96 %. F-PUSS demonstrates remarkable self-healing capabilities, with a healing efficiency of 78 % after 48 h at 60 °C. This study provides valuable insights for designing multifunctional polymer materials with anti-fouling, anti-corrosion, and self-healing functions.

Doping and Superhydrophobic Modification for Improving Marine Antifouling Performance of Alkali-Based Geopolymer Coating

Doping and Superhydrophobic Modification for Improving Marine Antifouling Performance of Alkali-Based Geopolymer Coating

Superamphiphilic aerogels with 2D lamellar structure of gelatin-tuned 3D supramolecular network of collagen fibers for high-performance separation of surfactant-stabilized emulsified oily wastewater

Superwetting aerogel is a promising alternative for the remediation of emulsified oily wastewater for its high porosity combined with extreme wettability enabled high separation performances to emulsion wastewater. However, it remains challenging for superwetting aerogels to accomplish high-performance dual separation to surfactant-stabilized oil-in-water (O/W) and water-in-oil (W/O) emulsions with high stability. Herein, an environmentally benign superamphiphilic composite aerogel was prepared by a green synthesis route that relied on the utilization of natural amphiphilic biomass. Collagen fibers (CFs) were utilized to construct the three-dimensional (3D) supramolecular skeleton of aerogel to provide high storage capacity of water/oil and outstanding capillary effect to boost the mass transfer. The two-dimensional (2D) lamellar structure of gelatin (Gel) was further grown on the skeleton of CFs aerogel to play the role for simultaneously enhanced demulsifying capability and spreading of emulsions. The as-prepared superamphiphilic aerogel enabled the separation of highly stable surfactant-stabilized O/W and W/O emulsions with high separation efficiency and flux. Excellent recycling performances and anti-fouling performance were also confirmed. Our investigations therefore demonstrated that the structural engineering of superamphiphilic aerogel is a promising way to realize high-performance dual separation of surfactant-stabilized O/W and W/O emulsion wastewater.Graphical

In situ polymerization of a poly(3,4-ethylenedioxythiophene):poly(sodium–styrennesulfonate) conductive layer for electro-assisted ultrafiltration and fouling mitigation

Electrification can enhance the antifouling performance of ultrafiltration membranes and improve the sustainability of membrane technologies. The design of high-performance conductive membrane materials remains one of the core technologies in electro-assisted ultrafiltration. Here, conductive PVDF/PEDOT:PSS composite membranes were prepared via in situ chemical oxidation polymerization on a PVDF surface. The PVDF/PEDOT:PSS membranes were subsequently used for electro-filtration to study the effect of the applied potential on humic acid fouling. When a voltage of 3 V was applied, the PVDF/PEDOT:PSS20 membrane was continuously polluted for 5 cycles. The results showed that after simple hydraulic cleaning, the membrane flux recovery rate reached 91 %. Compared with that of the PVDF membrane, the irreversible fouling of the PVDF/PEDOT:PSS20 membrane decreased by 65 %. The modified Poisson Boltzmann equation indicates that applying cathodic potential on the surface of PEDOT:PSS conductive layer increases the cumulative concentration of counter ions on the membrane surface and the thickness of the charged layer, thereby promoting the migration of peak forces on the membrane surface to the bulk solution, changing the fouling behaviour of HA from cake filtration to standard blocking.

AgNP-doped cellulose acetate-based nanofiltration membrane for enhancing antifouling performance and separation of dye and salt

AgNP-doped cellulose acetate-based nanofiltration membrane for enhancing antifouling performance and separation of dye and salt

A novel nanofiltration membrane with a dual-charged layer to simultaneously remove anions and cations from acid mine drainage

A novel nanofiltration (NF) membrane with a positively and negatively dual-charged layer was finely designed in this study. The membrane was prepared by co-deposition of 4-tert-butylpyrocatechol (TBC) and polyethyleneimine (PEI) and electrostatic interaction to assemble positively and negatively charged functional layers on a substrate which is polyamide (PA)-based NF membrane. The NF membrane achieved excellent retention capacity through the combined effects of Donnan repulsion and electrostatic field trapping. The prepared membrane had a dense but thin surface layer with an average pore size of 0.84 nm, enabling an improved membrane flux of 8.66 L/(m2·h·bar) and high rejection to divalent inorganic salt ions (93.56 % Mg2+, 99.56 % SO42-). The membrane was used to treat acid mine drainage (AMD) and achieved an excellent retention capacity for ions in AMD (93.25 % Mg2+, 91.58 % Ca2+, 94.22 % Mn2+, 95.96 % SO42-), meeting industrial wastewater discharge standards. In addition, the NF membrane demonstrated good anti-fouling performance during the AMD treatment and significant potential for environmental remediation applications.

Construction of CS-SDAEM long-chain polysaccharide derivative on TA@CNTs coated PVDF membrane with effective oil-water emulsion purification and low contamination rate

Currently, the most effective way to improve the anti-fouling performance of water treatment separation membrane is to enhance the hydrophilicity of the membrane surface, but it can still cause contamination, leading to the occurrence of flux reduction. The construction of a strong hydration layer to resist wastewater contamination is still a challenging task. In this study, a defect-free hydration layer barrier was achieved by grafting chitosan polysaccharide derivatives (CS-SDAEM) on the membrane, which achieved in effective fouling prevention and low flux decline rate. A layer of tannic acid-coated carbon nanotubes (TA@CNTs) has been uniformly deposited on the commercial PVDF membrane so that the surface was rich in -COOH groups, providing sufficient reaction sites. These reactive groups facilitate the grafting of amphiphilic polymers onto the membrane. This modification strategy achieved in enhancing the antifouling performance. The modified membrane achieved low contamination rate with DR of 16.9 % for wastewater filtration, and the flux recovery rate was above 95 % with PWF of 1100 (L·m−2·h−1). The membrane had excellent anti-fouling performance, which provided a new route for the future development of water treatment membrane.

Study of the dual role mechanism triggered by in-situ cross-linking in hollow fiber membrane matrix

In this paper, a novel polyvinylidene fluoride (PVDF) hollow fiber membrane with uniform pore size and hydrophilic cross-linked network in membrane matrix was developed by non‐solvent induced phase separation method. The dual role mechanism of in-situ cross-linking in regulating molecular chain arrangement during phase separation and preventing deterioration of membrane mechanical properties were analyzed. The results demonstrated that the cross-linked network formed by in-situ crosslinking entangled with PVDF molecular chains which improved the regularity of PVDF molecular chains, increasing the uniformity of the pore size distribution, the percentage of the most probable pore size of the modified membrane increased to 93.25 %. The cross-linked network was immobilized in the membrane which formed semi-interpenetrating structure, maintaining the mechanical properties of the membrane. The permeation flux of the modified membrane increased by 24.1 times to 477.7 L m−2 h−1 compared to the original PVDF membrane. The rejection of BSA was maintained at 98.5 %, with the tensile strength increased to 2.52 MPa. The modified membrane exhibited persistent hydrophilicity in 21 days washing experiment with improved antifouling performance.

Block copolymer brushes modified cotton fabric for antifouling oil-water separation materials with thermal responsiveness

Polymer brushes have proven to have great potential in oil-water separation but it remains a long-standing challenge to improve their operational stability and service endurance. In this work, we sequentially grafted polydimethylsiloxane (PDMS) and poly (N-isopropylacrylamide) (PNIPAM) brushes on the cotton fabric to prepare a durable and self-reparing oil-water separation film (Co@PDMS/PNIPAM). The grafting of liquid PDMS brushes significantly improved the antifouling performance through its lubricating effect thereby improving the durability. The hydrophilic and thermoresponsive PNIPAM was synthesized through a surface-initiated atom transfer radical polymerization (SI-ARGET ATRP). Co@PDMS/PNIPAM shows high flux in various oily water and bio-solution. More remarkably, Co@PDMS/PNIPAM exhibited intelligent self-repairing characteristics, and this further enhances its stability and service endurance in the application of oil-water separation. The results provide pathways to the preparation of antifouling and durable membranes in the application of water treatment, and resource recovery.

Eco-friendly, highly interpenetrated and slightly swollen pHEMA hydrogel foam for durable underwater superoleophobicity and emulsion separation

Despite the emergence of hydrogels as ideal candidates for preparing the superhydrophilic materials for emulsion separation, their structural stability and swelling still hinder their long-term use, mainly due to structure defects after swelling. Herein, differing from the common modification, the eco-friendly poly 2-hydroxyethyl methacrylate (pHEMA) hydrogel foam was designed and synthesized via a one-step strategy by using the high internal phase emulsion (HIPE) template method, which endowed it with a highly interpenetrated porous structure. Unlike the normal swellable hydrogels such as poly(N-isoproplyacrylamide) (PNIPAM) hydrogel, or modified hydrogel coatings, the pHEMA hydrogel foam displayed stable structure and underwater superoleophobicity after 20 d of immersion in water. The pHEMA hydrogel foam could separate different kinds of highly surfactant-stabilized oil-in-water (O/W) emulsions with a high separation efficiency of 99.3% for liquid paraffin emulsion obtained solely under gravity-driven. Additionally, it exhibited excellent antifouling performance and long-term acid/alkali tolerance over 100 h without decrease in emulsion separation efficiency (98.0%, oil/water ratio of 99:1) and permeation flux (over 2000 L·m−2·h−1) attributed to its stable bulky structure. Moreover, the pHEMA hydrogel foam demonstrated high cell viability of 96.87% and 95.96% after culturing the 3T3 clone A31 cells in the pHEMA hydrogel foam for 24 h and 48 h, respectively, indicating good biocompatibility. Hence, our work provides a new design to develop an eco-friendly bulk hydrogel foam that achieves stable structure and performance for emulsion separation.

Marine Fouling Release Performance of Amphiphilic Carboxybetaine Perfluoropolyether Methacrylate Polymer Coatings

AbstractAmphiphilic polymer systems have been demonstrated to be an effective and environmentally friendly approach to combat the challenges of biofouling, especially in the real ocean environment. A variety of polymer compositions containing fluorophilic perfluoropolyether (PFPE) urethane dimethacrylate and zwitterionic carboxybetaine methacrylate (CBMA) are in situ copolymerized across a broad concentration range and anchored to chemically functionalized substrates by grafting‐through polymerization. Dynamic accumulation assays with the marine diatom Navicula perminuta and the marine bacterium Cobetia marina revealed an enhanced antifouling performance in most of the amphiphilic polymer mixtures when zwitterionic units are combined with hydrophobic PFPE compounds. It is noticed that the resulting polymer networks still possess enough orientational freedom to quickly rearrange in the presence of water. It is further observed that several of the very hydrophilic formulations and some of the moderately hydrophobic formulations exhibit low fouling against the marine fouling organisms Navicula perminuta and Cobetia marina. This correlated with increased surface roughness and the ability for underwater rearrangement. Furthermore, it is discussed whether the probability that highly hydrated hydrogels, which appear sponge‐like, may create a diffuse interphase which promotes the incorporation of silt. Latter is counteracted by the hydrophobic PFPE building blocks in the amphiphilic coatings.

An electrospun iron oxychloride/polyacrylonitrile nanofibrous membrane with superhydrophilic and excellent regeneration properties: Achieving superior oil-in-water emulsion separation

Superhydrophilic polymer membranes are widely used in oil-water separation due to their excellent wettability, high efficiency, low cost, and good biocompatibility. However, challenges such as fouling adhesion and inadequate stability persist during the treatment of oily wastewater. Herein, a novel iron oxychloride/polyacrylonitrile (FeOCl/PAN) nanofibrous membrane with superhydrophilicity and remarkable regenerability was successfully fabricated through simple electrospinning technique, which maintained good physicochemical stability under various harsh conditions with the uniform distribution of FeOCl on PAN fibers. The surface morphology and chemical compositions of the optimized FeOCl/PAN membrane were studied by several characterization techniques. The introduced FeOCl nanocrystals through electrospinning endowed the membrane with a rougher surface structure, significantly improving the hydrophilicity of the FeOCl/PAN nanofibrous membrane. In the cross-flow isooctane-in-water emulsion separation experiment, the initial water flux recovery rate (FRR) of the membrane increased from 92 % for the pure PAN membrane to around 99 %. Meanwhile, the optimized FeOCl/PAN nanofibrous membrane achieved an emulsion (isooctane) flux of approximately 632.9 L m−2 h−1, with an oil droplet removal rate surpassing 99.4 %. Furthermore, by cleaning the membrane with H2O2 (60 mM, pH = 3), the FeOCl/PAN membrane exhibited an exceptionally high water flux recovery rate (∼100 %) after high-concentration paraffin-in-water emulsion (4000 mg L−1) separation. In addition, the FeOCl/PAN membrane also demonstrated excellent antifouling performance in bovine serum albumin (BSA) pollution experiment. In summary, this work might provide a unique strategy for preparing advanced functional membranes with superior efficiency and durability for emulsified oily wastewater treatment.

Cross-scale interface engineering strategy to achieve self-healing antifouling material strength and toughness symbiosis

The incorporation of self-healing technology into antifouling coatings is crucial for the extension of their service life and durability. However, the challenge lies in the insufficient coexistence of strength and toughness hinders their long-term serviceability. Here, this study proposes a cross-scale interfacial engineering strategy for self-healing antifouling coatings inspired by the multiscale microstructure of natural biomaterials The strategy involves the in-situ growth of antifouling zinc-based metal–organic frameworks (Zn-MOF) within a self-healing polymer network constructed by multiple hydrogen bonds. The synergistic cross-scale interfacial interactions between Zn-MOF and the polymer molecules, combined with the intrinsic antifouling properties of Zn-MOF, significantly enhance the strength, toughness to 27.48 MPa, 277.81 MJ/m3, and benefit improving antifouling performance. Moreover, the molecular integration of Zn2+-pyridine coordination optimizes the microphase structure of the polymer matrix and embeds the advantage of its fast damage response, thereby further enhancing the robustness, and reaching self-healing efficiency to 91.74 % at 40 °C for 24 h. Overall, the proposed strategy represents a viable approach for the fabrication of highly resilient and tough self-healing antifouling coatings.

Polyvinylidene fluoride-based loose nanofiltration membrane with graphene oxide intercalation for efficient small organic molecules desalination

Graphene oxide (GO) loose nanofiltration (LNF) membranes show immense potential for the desalination of small organic molecules. However, it remains a significant challenge to compare the performance of GO LNF membranes prepared via different doping methods and study the mechanisms that influence the separation abilities of the membranes. In this study, LNF membranes prepared via three GO doping methods were examined for flux, retention rate, and the separation performance of small organic molecules and inorganic salts. The membranes coated with dopamine (DA) and GO, and subsequently formed polydopamine (PDA)–GO intercalation, showed the best results. A novel LNF membrane material (PVDF/PDA–GO–TFN; PVDF: polyvinylidene fluoride, TFN: thin-film nanocomposite) was developed to enhance the separation performance of small organic molecules and inorganic salts while improving membrane surface stabilization and anti-fouling performance and reducing the “trade-off” effect. The optimal conditions for PDA–GO intercalation and the best combination for interfacial polymerization (IP) were also determined. The intercalation structure was identified via scanning electron microscopy coupled with energy-dispersive X-ray spectroscopy, atomic force microscopy, and Fourier-transform infrared spectroscopy. Furthermore, the separation mechanism of the membrane was determined to be based on the Donnan and steric hindrance effects, according to the correlation analysis of the membrane surface electrical properties (zeta potential), hydrophilicity (contact angle), and pore properties. The PVDF/PDA–GO–TFN LNF membrane displayed a maximum water permeance of 10.45 L/(m2·h·bar), with an 88 % rejection of PEG2000 and a 6.83 % rejection of Na2SO4. Moreover, the membrane exhibited excellent anti-fouling performance and long-term stability, with a mean flux recovery rate of 99.06 % after four cycles of filtration and backwashing tests using small organic molecules and inorganic salt solutions. The inorganic salt retention rate was analyzed using SPSS software, and the results indicated excellent membrane stability. In summary, the preparation of PVDF/PDA–GO–TFN membrane materials provides a novel approach for fabricating LNF membranes that can effectively separate small organic molecules and inorganic salts.

Performance of capacitive deionizing membrane distillation (CDIMD) process for the organic sewage treatment and how operating parameters can affect it

To solve the fouling issue of traditional membrane distillation (MD) technique, a newly-designed hybrid purification system integrating capacitive deionization (CDI) with MD technology was established for the organic sewage treatment in this study, namely capacitive deionizing membrane distillation (CDIMD) technology. Complexes formation via cross-linking among protein, divalent cations, and polysaccharide, an archcriminal inducing MD fouling, was remarkably alleviated in the CDIMD system considering that negatively-charged organics were clearly divided away from those divalent cations in an electric field circumstance. The CDIMD performance was deeply explored in this study focusing on the impact mechanisms of core operational parameters. An appropriate increment of feed temperature (60–65 °C) and feed flow velocity (15.72–17.82 mm/s) contributed to the anti-fouling performance of CDIMD. Considering the side reactions at voltage >1.2 v, setting working voltage at around 1.2 v seemed to be optimal for CDIMD operation. With an overall consideration of pure water production and anti-fouling performance, a properly thicker CNTs layer (40–60 μm) efficiently enhanced the fouling mitigation of CDIMD. A frequent switching of electric field direction (9/1 min) facilitated the timely regeneration of electrode and composite membranes, accordingly promoting a reliable purification of organic wastewater by CDIMD technique.