Jia-qi LI, Chuan-jie FANG, Wei-lin FENG, Jin-chao FANG, Li-ping ZHU

Surface/Interfacial design and tailoring of polymeric membranes for liquid-phase separation*

Jia-qi LI, Chuan-jie FANG, Wei-lin FENG, Jin-chao FANG, Li-ping ZHU??

?E-mail: lpzhu@zju.edu.cn

Synthetic polymer membranes are widely used in many applications, including, among others, water purification, protein separation, and medicine. However, the use of existing polymer membranes faces major challenges, such as the trade-off between permeability and selectivity, membrane fouling, and poor mechanical strength. To address these problems the authors have focused their research on surface/interfacial tailoring and the structure-property relationship of polymer membranes used in liquid separation systems. Progress has been made as follows: (1) a methodology for membrane surface functionalization and nanofiltration (NF) membrane preparation based on mussel-inspired catecholic chemistry was proposed and established; (2) a class of mechanically robust and environmentally-responsive composite membranes with hydrogel pore-filled in rigid macroporous supports was designed and developed; (3) a methodology for surface tailoring and antifouling modification of polymer membranes based on amphiphilic copolymers was created and the scientific implications for amphiphilic polymer membranes elaborated; (4) an adsorption membrane with both filtration and adsorption functions was designed and developed to achieve rapid removal of trace micropollutants, including heavy metal ions, organic dyes, plasticizer, antibiotics, and others. This mini-review briefly summarizes this work.

Separation membranes; Amphiphilic copolymer; Catecholic chemistry; Antifouling; Adsorption membranes

1 Introduction

Synthetic polymer-based separation membranes are used in a wide variety of applications, including water treatment, protein and drug concentration, food processing, batteries and fuel cells, gas separation, air filtration, medical health, and more (Park et al., 2007; Lee et al., 2014; Mohammad et al., 2015; Tan et al., 2018). However, the existing utilization of synthetic membranes faces challenges such as the trade-off between permeability and selectivity, membrane fouling, and a complicated manufacturing process. Designing and preparing high performance (high permselectivity, antifouling, high strength, chemical stability, energy-efficiency, etc.) and multi-functional (stimuli-responsive, biocompatible, or catalytic) membranes is a significant priority in driving the development and application of membrane technology. The aim of this mini-review is to summarize our recent work on surface/interfacial design and the tailoring of traditional and novel polymer membranes used in liquid separation systems.

2 Membrane surface tailoring and functionalization based on mussel-inspired catecholic chemistry

As a versatile tool for manipulating material properties, mussel-inspired catecholic chemistry has recently become an interdisciplinary research topic of strong interest in material science, chemistry, and biomedicine. Some studies have shown that dopamine, a catecholic biological neurotransmitter widely existing in living organisms, is able to behave like mussel foot proteins in the byssal plaque of Mytilus (Fig. 1) (Zhang et al., 2017c). It undergoes oxidative self-polymerization in an alkaline aqueous solution and creates a polydopamine (PDA) coating that adheres firmly to various solid surfaces. In 2008, the authors used this strategy for the first time to perform surface chemical modification and functionalization of polymer membranes (Xi et al., 2009). Hydrophobic porous membranes were successfully hydrophilized by a simple dip-coating process with a dopamine or 3,4-dihydroxy-L-phenylalanine (L-DOPA) aqueous solution under weak alkaline conditions. The water permeability of the polymer membranes was improved by 64%. This provided a convenient method for surface modification of various polymer membranes (Xi et al., 2009).

The evolution of dopamine in the solution as well as the surface characteristics of the PDA layer on various substrates were investigated in detail, and a primary model on PDA adsorption and deposition on solid surfaces was proposed. It was found that PDA oligomers were first obtained in solution by oxidation, cyclization, and molecular rearrangements. Then, the oligomers were adsorbed, aggregated, and deposited onto substrate surfaces by non-covalent interactions (Fig. 2) (Jiang et al., 2011; Zhang et al., 2017c). This explanation concurs with that of the J.L. Lenhart group from the U.S. Army Research Laboratory (Knorr Jr et al., 2016).

Despite its advantages for membrane surface modification, PDA deposition shows some shortcomings, such as long-time consumption, high surface roughness, and weak alkaline resistance. In order to accelerate the formation of catecholic thin films instead of pure PDA, metal-phenolic network films were constructed on substrate via rapid complexation of Fe(III) ions with PDA oligomers or tannic acid. The deposition process was shortened significantly to several minutes and smoother surfaces were obtained (Lin et al., 2018; Zhang PB et al., 2019). In addition, PDA nanoparticles (NPs) were prepared by dopamine oxidation and self-polymerization. The sizes and morphologies of NPs were regulated by reaction parameters, including oxidant type, pH, reaction time, temperature, and others. The synthesized NPs were used as an additive of polymer membranes prepared by phase inversion or interfacial polymerization (Jiang et al., 2014; Zhang LL et al., 2019). It was found that both the hydrophilicity (water contact angle from 95.5° to 59.1°) and water permeability (improved by 1300%) for the membranes were greatly improved due to the incorporation of hydrophilic PDA NPs. These strategies can be extended to more polymers and catecholic substances and allow exploitation of novel functional composites.

Fig. 1 Mussel-bioinspired dopamine for material surface tailoring. Reprinted from (Zhang et al., 2017c), Copyright 2017, with permission from Journal of Functional Polymers

Fig. 2 Schematic diagram of PDA deposition on substrate surface. Reprinted from (Zhang et al., 2017c), Copyright 2017, with permission from Journal of Functional Polymers

The PDA films and aggregates containing reactive groups such as quinonyl, amine, and catecholic groups provide a versatile platform for further chemical tailoring and functionalization of membrane surfaces. A series of biopolymers or biomolecules —such as heparin, bovine serum albumin, and polymer brushes—were immobilized onto polymer membranes with an attached PDA coating or entrapped PDA NPs as the active intermediator to improve the biocompatibility or hemocompatibility of the membranes (Jiang et al., 2010, 2015; Zhu et al., 2011). In addition, polyvinyl pyrrolidone-iodine (PVP-I) was incorporated with polypropylene porous membranes by strong noncovalent interaction between PVP-I and PDA. This resulted in a significant improvement in the antifouling (permeation decay from 12.4% to 50.4%) and antibacterial (99.9% ofwere killed) properties of membrane surfaces (Jiang et al., 2013). In recent research, we reported surface fractal patterns created by the dynamic assembly of PDA nanoaggregates. Mineralization or metal deposition was used to keep the pattern fixed and maintain particular functionalities. This strategy of material surface patterning is applicable to a broad range of materials which allows the development of materials with controllable patterned structures (Zhang et al., 2017b). Moreover, the modified materials mediated by PDA have potential applications in oil/water separation, separation for lithium ion batteries, and more (Zhang PB et al., 2018, Zhang Y et al., 2018).

Hierarchically self-assembled and microporous characteristics make possible the application of PDA coating in nanofiltration. We successfully prepared a thin-film composite (TFC) membrane by depositing PDA layers on polysulfone ultrafiltration (UF) membranes. The obtained composite membranes exhibited a characteristic of positively charged NF membranes—they could completely reject the brilliant blue and Congo red dyes completely in water. This work is the first report on PDA nanofiltration (NF) membranes (Li et al., 2012). We further developed a strategy to improve the alkaline resistance of PDA NF membranes by the co-deposition of poly(ethylene imine) (PEI) and PDA followed by a crosslinking step (Zhang et al., 2017a). Moreover, the NF performances of PDA TFC membranes were further optimized by reaction conditions, such as extra amine sources, and additional crosslinked process (Tang et al., 2018; Li et al., 2019).

In summary, we performed a systematic study on the preparation and functionalization of polymer separation membranes based on mussel-inspired catecholic chemistry, and established a methodology for membrane surface functionalization and NF membrane preparation based on mussel-inspired surface chemistry. We described self-polymerization and the evolution of the typical catecholic substance, dopamine, in aqueous solutions, and we proposed a primary model on PDA adsorption and deposition on solid surfaces in solution. TFC NF membranes with PDA-based film as the selective layer were developed and used for molecular separation in liquids. Furthermore, surface functionalization of polymer membranes was performed through a secondary surface reaction with PDA as an intermediate layer. Some applications of functionalized membranes can be found in molecular filtration, protein separation, blood purification, oil/water separation, separation for lithium-ion batteries, and other fields. This mini- review offers a versatile approach for membrane surface functionalization and NF membrane preparation.

3 Design and development of amphiphilic copolymer membranes

Membrane fouling is one of the key challenges in membrane separation applications. Traditional polymer membranes are often susceptible to membrane fouling due to their hydrophobic character and low surface energy. Amphiphilic macromolecules simultaneously containing hydrophobic and hydrophilic chains in their molecular structure demonstrate great potential for integrating the advantages of hydrophobic and hydrophilic polymers in membranes. In our work to develop polymer membranes with strong antifouling properties and high mechanical strength, a series of amphiphilic copolymers with various topological architectures were designed through the blending of additives of polyvinylidene fluoride (PVDF), polysulfone (PSF), polyethersulfone (PES), and ultra-/micro-filtration membranes prepared through the phase inversion process. We investigated in detail the effects of amphiphilic macromolecules on membrane morphologies and properties. The hydrophilic chains in amphiphilic macromolecules are often immiscible with host polymers and thus are segregated onto membrane surfaces spontaneously during membrane formation. The hydrophobic part is generally miscible with the host polymer and anchored onto the membrane surface. As a result, hydrophilic and antifouling polymer brushes were immobilized onto membrane surfaces by a one-step process and the hydrophilicity and antifouling abilities of the membranes were significantly improved without sacrificing mechanical strength. Membrane flux modified by the hydrophilic polymer was improved by approximately two orders of magnitude, while antifouling ability was improved by approximately 100% (Yi et al., 2012a, 2012b, 2014b; Zhu et al., 2014a, 2014b).

Zwitterionic polymers are a class of well-known biomaterials with excellent antifouling properties due to their strong affinity with water molecules. Amphiphilic copolymers with zwitterionic chains are a strong candidate as the additive of phase inversion membranes to improve the antifouling ability of the membranes. However, a challenge for the application of zwitterionic copolymers is their low solubility in membrane-forming solvents such as,-dimethylacetamide (DMAc), and,-dimethylformamide (DMF), and thus their use in direct blending is difficult. In order to address this problem, the authors proposed a strategy based on secondary surface reaction from reactive amphiphilic copolymers blended in polymer membranes. First, nonionic amphiphilic copolymers containing tertiary amine groups were designed and synthesized. Then, the copolymers were used as the blend additive of phase inversion membranes. Finally, the surface-enriched tertiary amine groups were quaternized with 3-bromopropionic acid (3-BPA) or 1,3-propane sultone (Fig. 3). The generated zwitterionic poly(carboxybetaine methacrylate) or poly(sulfobetaine methacrylate) chains showed excellent antifouling ability for the polymer membranes (Zhao et al., 2013, 2014a, 2014b, 2015; Zhu et al., 2014a, 2014b).

Stimuli-responsivity is an attractive characteristic for polymeric membranes used in chemical separation, drug delivery, biomedical fields, and other areas. Stimuli-responsive membranes, which are composed of the membrane matrix and stimuli- responsive functional gates, can switch their permeability and separation properties in response to environmental stimuli, such as temperature, pH, ionic strength, light, electric, and magnetic fields. In the work of the authors’ group, amphiphilic copolymers containing stimuli-responsive polymer chains were designed, synthesized, and used for the preparation of stimuli-responsive membranes. It was demonstrated that the modified membranes showed stimuli- responsive characteristics in response to pH, temperature, inorganic salt, etc. The authors’ research team provided a simple and convenient strategy for the preparation of smart membranes (Yi et al., 2014a, 2015; Zhao et al., 2016).

Fig. 3 Schematic diagram of membrane surface zwitterionicalization based on amphiphilic copolymer blending

The self-assembly of amphiphilic block copolymers can also be used to prepare porous polymer membranes. Free-standing symmetrical porous membranes were prepared with a polystyrene-block- poly(4-vinylpyridine) (PS-b-P4VP) diblock copolymer by combining self-assembly and nonsolvent- induced phase separation (the SNIPS process). Uniform cylindrical micelles can be constructed from the amphiphilic block copolymer during the SNIPS process. The membranes displayed an impressive ultrastructure in the overlapping of the cylindrical micelles. The water permeability of the prepared membrane reached 400 L/(m2?h?bar) in neutral conditions (1 bar=1×105Pa). Significantly, when the pH of the feed solution changed from 1 to 6, the permeability and selectivity of the symmetrical membrane showed a strongly pH-dependent character. The potential application of the developed membranes in the size fractionation of NPs with a wide size distribution was demonstrated (Fig. 4) (Yi et al., 2016).

Based on the above-mentioned work, a methodology for surface tailoring and antifouling modification of polymer membranes based on amphiphilic copolymers was created and the scientific implications for amphiphilic polymer membranes were discussed. The mechanisms of surface segregation of amphiphilic macromolecules during membrane formation and application were shown. The obtained membranes, modified by amphiphilic copolymers, have been frequently applied in applications such as drinking water purification, wastewater treatment, and biomedical separation.

Fig. 4 pH-responsive PS-b-P4VP membranes used for nanoparticle size fractionation. Reprinted from (Yi et al., 2016). Copyright 2016, with permission from American Chemical Society

4 Design, development, and applications of gel-filled and adsorption membranes

Polymer hydrogels demonstrate strong potential in the preparation of separation membranes due to their unique mesh-like architecture and stimuli- responsive behavior. Based on a designable “hydrogel pore-filling” concept, a novel class of polymer composite membranes was developed by incorporating functional hydrogels into a porous support membrane. As a typical example, poly(-vinyl imidazole) (PVI) gel-filled composite membranes were synthesized by ultraviolet (UV)-initiated graft polymerization of a VI monomer with a crosslinking monomer from a UV-active asymmetric PSF UF support. These membranes with unique mesh-like architecture showed water permeance between ~0.5 and 10 L/(m2?h?bar) and pore size ranging from ~1.5 to 2 nm, depending on the PVI grafting degree. The rejections of different salts were in the order of MgCl2>NaCl?MgSO4>Na2SO4, suggesting that the rejection mechanism was dominated by Donnan exclusion (Cheng et al., 2015). In contrast to traditional NF membranes, three main mechanisms were involved in the separation: size exclusion (sieving), electrostatic repulsion (Donnan exclusion), and adsorption (involved in hydrophobic effect or electrostatic attraction). Significantly, PVI gel-filled membranes can indeed fractionate molecule mixture and molecule/salt mixture based on solute size and charge as well as on the solution condition. In particular, PVI gel-filled membranes show different pore sizes for molecular rejection in different pH conditions because of the stimuli-responsive behavior of polymer hydrogel (Cheng et al., 2016). Furthermore, a class of mechanically robust composite membranes containing polymer gels confined in the pores of rigid microporous supports has been developed and used for the rapid removal of organic pollutants such as various dyes from water through the flow-through adsorption process (Sun et al., 2016; Hu et al., 2017, 2018; Liu et al., 2017; Fang et al., 2018).

In our recent work, a crosslinked β- cyclodextrin-based polymer of intrinsic microporosity (β-CD-PIM) was designed and synthesized with the goal of removing persistent organic micropollutants—including plasticizers, pesticides, pharmaceuticals, and endocrine disrupters—from water, in an efficient and cost-effective way. The hierarchically micro-mesoporous structures and hydrophilic characteristics enable this polymer to adsorb a variety of organic pollutants from water with both at a very high rate and capacity. The maximum adsorption capacity for bisphenol A (BPA) reached 502 mg/g— approximately 5.7 times as large as that of the state- of-the-art porous β-CD polymer (Wang et al., 2019a, 2019b, 2020). A filtration membrane impregnated with a β-CD-PIM was able to remove>99.9% of BPA with a water permeability of a maximum of 1000 L/(m2?h?bar)—approximately 100 times greater than that of traditional NF membranes with similar functions. In addition, the membrane was easily regenerated and kept a high separation efficiency of over six adsorption-desorption cycles, exhibiting strong potential in water purification (Fig. 5) (Wang et al., 2019b).

A hydrogel in situ filling strategy was used to prepare a class of porous membranes for rapid removal of trace organic and inorganic micropollutants from water. In this technique, the hydrogel precursor was first prepared and then added into the cast solution of membranes. Subsequently, hydrogel in situ filling was conducted by further crosslinking and membrane casting. A hydrogel composite hollow fiber membrane was successfully prepared with a dry-wet spinning technique. These membranes can remove more than 99% of heavy metal ions and organic pollutants from water with a high water permeation. The separation mechanism was not attributed to size sieving or Donnan exclusion, but specifically to adsorption. The preparation of this membrane has been scaled up and a series of patents have been granted (Zhu et al., 2015a, 2015b, 2015c, 2015d). This membrane has been manufactured in large scale by the Ningbo Fotile Company, China and used in household water purifiers.

Fig. 5 PVDF/β-CD-PIM composite membrane for ultrafast removal of organic micropollutants using the flow-through adsorption process. Reprinted from (Wang et al., 2019b), Copyright 2019, with permission from Elsevier

(a) Schematic diagram of filtration and adsorption of the composite membrane; (b) Digital photograph of the composite membrane; (c) Cross-sectional SEM image of composite membrane; (d) Adsorption break-through curves of the composite membrane with various permeation fluxes; (e)Adsorption break-through curves of the composite membrane towards various single organic micropollutants

5 Summary and outlook

Membrane-based separation has been increasingly applied to address global challenges such as water scarcity, environmental pollution, industrial purification, energy storage and conversion, and health care. In our group, some advances have been made in performance improvements and multifunctionalities of traditional polymer membranes via surface/interfacial design and tailoring. The key problems, such as membrane fouling, the trade-off between permeability and selectivity, and low mechanical strength have been solved, to a certain extent. Such research is significant in its ability to propel the widespread application of membrane technologies, but much research remains to be done. To expand in new directions and remain economically viable, membrane development must seek higher performance and lower costs. In recent years, in order to break through the inherent limitations of conventional membrane materials, novel materials such as aquaporin, graphene, metal-organic frameworks, microporous organic polymers, and self-assembled block copolymers have been explored. In future research, attention should be paid to an in-depth understanding of transport and rejection mechanisms, as well as structure-property relationships. At present, these areas remain challenging. Molecular-level design and processing approaches to the fabrication of highly selective membranes should be developed. The importance to the practical application of membrane technology of the packing of membranes into optimized modules is also often neglected.

Contributors

Jia-qi LI wrote the first draft of the manuscript and revised the final version. Chuan-jie FANG revised and edited the final version. Wei-lin FENG and Jin-chao FANG processed the data curation, investigation, and visualization. Li-ping ZHU helped to organize the manuscript, and revised and edited the final version.

Conflict of interest

Jia-qi LI, Chuan-jie FANG, Wei-lin FENG, Jin-chao FANG, and Li-ping ZHU declare that they have no conflict of interest.

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題目：用于液相分離的聚合物膜表/界面的設(shè)計(jì)與剪裁

概要：合成聚合物分離膜被廣泛應(yīng)用于水處理、蛋白質(zhì)分離和醫(yī)療保健等領(lǐng)域。然而，傳統(tǒng)聚合物膜面臨著重大的挑戰(zhàn)，例如滲透性和選擇性之間相互制約、膜易被污染、機(jī)械強(qiáng)度低等。為了解決這些難題，本研究小組在聚合物分離膜的表/界面設(shè)計(jì)與剪裁以及膜材料構(gòu)效關(guān)系上進(jìn)行了系統(tǒng)的研究工作，并取得了以下進(jìn)展：（1）提出并建立了一種基于貽貝仿生兒茶酚化學(xué)的膜表面功能化與納濾膜制備新途徑；（2）設(shè)計(jì)并制備了一種以剛性多孔基膜為載體的凝膠填充聚合物復(fù)合膜，發(fā)展了一種高機(jī)械強(qiáng)度的環(huán)境響應(yīng)性分離膜制備方法；（3）建立了基于兩親聚合物的分離膜表面按需設(shè)計(jì)以及抗污改性的新方法；（4）設(shè)計(jì)并開發(fā)了一系列兼具過濾與吸附功能的吸附型分離膜，可用于水中痕量重金屬離子、抗生素、塑化劑等微污染物的快速脫除。

關(guān)鍵詞：分離膜；兩親聚合物；兒茶酚化學(xué)；抗污染；吸附膜

Dr. Li-ping ZHU has been the Editorial Board Member ofsince 2018. Dr. ZHU received his bachelor’s degree from Hunan University, China in 2001, and his PhD degree in polymer chemistry and physics from Zhejiang University, China in 2007. He worked on polymer chemistry and polymer membrane materials as a postdoctoral associate from 2007 to 2009 at Zhejiang University and has been employed as a faculty member from 2009 at the Department of Polymer Science and Engineering, Zhejiang University. He has been a visiting scholar at the University of California-Riverside and University of Pennsylvania, USA in 2011 and 2012–2013, respectively. Dr. ZHU has received funds for six research projects from the National Natural Science Foundation of China. To-date, he has published more than 130 peer-reviewed SCI-indexed journal papers and has been granted 24 patents. The total SCI-citation number of Dr. ZHU’s published papers is more than 4800 and his-index has reached 37. He was granted the Science & Technology Advancement Award (first prize) by the Government of Zhejiang Province in 2015 and the Science & Technology Advancement Award (first prize) by the Chemical Industry and Engineering Society of China in 2019, both in recognition of his important contributions to membrane science and technology.

https://doi.org/10.1631/jzus.A2000170

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*Project supported by the National Natural Science Foundation of China (Nos. 51828301, 51773175, and 51973185) and the Fundamental Research Funds for the Central Universities, China

? Zhejiang University and Springer-Verlag GmbH Germany, part of Springer Nature 2020

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