Evaluation of groundwater quality for drinking water using a quality index in Abyi Adi, Tigrai, Northern Ethiopia.

High quality, safe and sufficient drinking water is essential for public health and well-being. However, the war on Tigrai damaged the water sources of communities and pose people to health problems. Therefore, the aim of the present study was to assess the quality of water of the town of Abyi Adi, Tigrai, Northern Ethiopia using physicochemical and biological parameters and water quality indices. A total of 36 water samples were collected from four major water sources. The physicochemical and biological parameters were determined using standard analytical procedures for water analysis. The mean values of electrical conductivity and pH ranged from 273.63 to 881.27 µS/cm and 6.68 to 7.42, respectively. Moreover, the experimental results of major cations (Na+ = 3.70-14.77 mg/L and Ca2+ = 8.50-15.77 mg/L), and anions (HCO3 - = 21.52-40.77 mg/L, Cl- = 13.56-40.29 mg/L, NO3 - = 0.14-0.25 mg/L, NO2 - = 0.24-0.76 mg/L and PO4 3- = 0.34-1.32 mg/L) were recorded below the World Health Organization (WHO) permissible limits set for drinking water. The water quality index (WQI) that is determined using a weighted arithmetic water quality index method (WAWQIM) was also found in the range of 5.3-37.2. Subsequently, all groundwater sources except Adibakla are classified as excellent or "A" rating. However, the total coliform of Maylomin and Chiny water sources were found to be 6.33 MPN/100 mL and 3.67 MPN/100 mL, respectively. Both are higher than the WHO permissible limit set for drinking water. Considering the susceptibility of groundwater to pollution and its impact to human health, regular monitoring and supervision should be performed to keep the water safe for drinking. Accordingly, chlorination water treatment process is recommended to provide safe drinking water.

Waste-treating-waste: Effective heavy metals removal from electroplating wastewater by ladle slag.

Ladle slag, a by-product of steelmaking, presents a valuable strategy for waste reduction and valorization in wastewater treatment. This work demonstrates the successful simultaneous removal of Al(III), B(III), Ba(II), Cr(III), Mg(II), Sr(II), Pb(II), and Zn(II), from electroplating wastewater by ladle slag. First, Cr(III) and Pb(II) removals were evaluated in single synthetic systems by analyzing the influence of pH, temperature, and ladle slag dosage. Competitive removal was observed in binary batch experiments of Cr(III) - Pb(II), achieving 88% and 96% removal, respectively, with fast kinetics following a pseudo-second-order model. The findings of XRD, SEM, EDX, and FTIR of the slag after removal helped to elucidate the synergic removal mechanism involving ladle slag dissolution, precipitation, ion exchange, and adsorption in a tight relationship with the solution pH. Lastly, ladle slag was tested in real electroplating wastewater with the aforementioned ions at concentrations ranging from <1 to 1700 mg/L. The removal was performed in two steps, the first attained the following efficiencies: 73% for Al(III), 88% for B(III), 98% for Ba(II), 80% for Cr(III), 82% for Mg(II), 99% for Pb(II), 88% for Sr(II), and 88% for Zn(II). Visual MINTEQ simulation was utilized to identify the different species of ions present during the removal process. Furthermore, the leaching tests indicated a minimal environmental risk of secondary pollution in its application. The results promote an effective and sustainable approach to wastewater treatment within the circular economy.

Synergistic interfacial polymerization between hydramine/diamine and trimesoyl chloride: A novel reaction for NF membrane preparation.

Polyester-amide (PEA) thin film composite (TFC) NF membranes have rapidly evolved towards a competitive performance, benefiting from their remarkable antifouling capability and superior chlorine resistance. In this report, a new concept of synergistic interfacial polymerization is explored, which promptly triggers the reaction between hydramines and trimesoyl chloride (TMC) in the presence of a trace amount of diamines. This rapid-start mode enables the formation of defect-free PEA films without the requirement of catalysis. A comprehensive characterization of physicochemical properties using high-resolution mass spectrometer (HRMS) reveals that the recombination and formation of a "hydramine-diamine" coupling unit plays a decisive role in activating the synergistic interfacial polymerization reaction with TMC molecules. Taking the pair of serinol and piperazine (PIP) as an example, the PEA-NF membrane fabricated with 0.1 w/v% serinol mixed with 0.04 w/v% PIP as water-soluble monomer and 0.1 w/v% TMC as oil phase monomer was found to have a pure water permeability (PWP) of 18.5 L·m-2·h-1·bar-1 and a MgSO4 rejection of 95.5 %, which surpasses almost all the reported PEA NF membranes. Findings of the current research provide more possibilities for the low-cost and rapid synthesis of high-performance PEA membranes aiming for water purification.

Contrasting mixed scaling patterns and mechanisms of nanofiltration and membrane distillation.

Oriented towards the pressing needs for hypersaline wastewater desalination and zero liquid discharge (ZLD), the contrasting mixed scaling of thermal-driven vacuum membrane distillation (VMD) and pressure-driven nanofiltration (NF) were investigated in this work. Bulk crystallization was the main mechanism in VMD due to the high salinity and temperature, but the time-independent resistance by the adsorption of silicate and organic matter dominated the initial scaling process. Surface crystallization and the consequent pore-blocking were the main scaling mechanisms in NF, with the high permeate drag force, hydraulic pressure, and cross-flow rate resulting in the dense scaling layer mainly composed of magnesium-silica hydrate (MSH). Silicate enhanced NF scaling with a 75% higher initial flux decline rate attributed to the MSH formation and compression, but delayed bulk crystallization in VMD. Organic matter presented an anti-scaling effect by delaying bulk crystallization in both VMD and NF, but specifically promoted CaCO3 scaling in NF. Furthermore, the incipient scaling was intensified as silicate and organic matter coexisted. The scaling mechanism shifted from surface to bulk crystallization due to the membrane concentration in both VMD and NF. This work fills the research gaps on mixed scaling mechanisms in different membrane processes, which offers insights for scaling mitigation and thereby supports the application of ZLD.

Polyphenol-mediated defect patching of graphene oxide membranes for sulfonamide contaminants removal and fouling control.

Graphene oxide (GO)-based laminar membranes are promising candidates for next-generation nanofiltration membranes because of their theoretically frictionless nanochannels. However, nonuniform stacking during the filtration process and the inherent swelling of GO nanosheets generate horizontal and vertical defects, leading to a low selectivity and susceptibility to pore blockage. Herein, both types of defects are simultaneously patching by utilizing tannic acid and FeⅢ. Tannic acid first partially reduced the upper GO framework, and then coordinated with FeⅢ to form a metal-polyphenol network covering horizontal defects. Due to the enhanced steric hindrance, the resulting membrane exhibited a two-fold increase in sulfonamide contaminants exclusion compared to the pristine GO membrane. A non-significant reduction in permeance was observed. In terms of fouling control, shielding defects significantly alleviated the irreversible pore blockage of the membrane. Additionally, the hydrophilic metal-polyphenol network weakened the adhesion force between the membrane and foulants, thereby improving the reversibility of fouling in the cleaning stage. This work opens up a new way to develop GO-based membranes with enhanced separation performance and antifouling ability.

High-Performance Bioinspired Microspheres for Boosting Dental Adhesion.

Dental adhesives are widely used in daily practice for minimally invasive restorative dentistry but suffer from bond degradation and biofilm attack. Bio-inspired by marine mussels having excellent surface-adhesion capability and high chemical affinity of polydopamine (PDA) to metal ions, herein, experimental zinc (Zn)-containing polydopamine-based adhesive formulation, further being referred to as "Zn-PDA@SiO2"-incorporated adhesive is proposed as a novel dental adhesive. Different Zn contents (5 and 10 mm) of Zn-PDA@SiO2 are prepared. Considering the synergistic effect of Zn and PDA, Zn-PDA@SiO2 not only presents excellent antibacterial potential and notably inhibits enzymatic activity (soluble and matrix-bound proteases), but also exhibits superior biocompatibility and biosafety in vitro/vivo. The long-term bond stability is substantially improved by adding 5 wt% 5 mm Zn-PDA@SiO2 to the primer. The aged bond strength of the experimentally formulated dental adhesives applied in self-etch (SE) bonding mode is 1.9 times higher than that of the SE gold-standard adhesive. Molecular dynamics calculations indicate the stable formation of covalent bonds, Zn-assisted coordinative bonds, and hydrogen bonds between PDA and collagen. Overall, this bioinspired dental adhesive provides an avenue technology for innovative biomedical applications and has already revealed promising perspectives for dental restorative dentistry.

Green Synthesis of Cation Exchange Membranes: A Review.

Cation exchange membranes (CEMs) play a significant role in the transition to a more sustainable/green society. They are important components for applications such as water electrolysis, artificial photosynthesis, electrodialysis and fuel cells. Their synthesis, however, is far from being sustainable, affecting safety, health and the environment. This review discusses and evaluates the possibilities of synthesizing CEMs that are more sustainable and green. First, the concepts of green and sustainable chemistry are discussed. Subsequently, this review discusses the fabrication of conventional perfluorinated CEMs and how they violate the green/sustainability principles, eventually leading to environmental and health incidents. Furthermore, the synthesis of green CEMs is presented by dividing the synthesis into three parts: sulfonation, material selection and solvent selection. Innovations in using gaseous SO3 or gas-liquid interfacial plasma technology can make the sulfonation process more sustainable. Regarding the selection of polymers, chitosan, cellulose, polylactic acid, alginate, carrageenan and cellulose are promising alternatives to fossil fuel-based polymers. Finally, water is the most sustainable solvent and many biopolymers are soluble in it. For other polymers, there are a limited number of studies using green solvents. Promising solvents are found back in other membrane, such as dimethyl sulfoxide, Cyrene™, Rhodiasolv® PolarClean, TamiSolve NxG and γ-valerolactone.

Making waves: Magneto-responsive membranes with special and switchable wettability: new opportunities for membrane distillation.

Membrane distillation (MD) has promising potential in the water purification and wastewater treatment industries; however, fouling and wetting are the main obstacles to its commercialization, and higher fluxes and energy efficiencies are essential. Magneto-responsive membranes (MagMem) with integrated magnetic nanoparticles (MNPs) enable in situ fouling mitigation and switchable separation by nano-mixing or nano-heating, triggered by external magnetic fields, in a range of membrane processes, but not yet been demonstrated in MD. This perspective discussed the potential paths of MagMem utilization in MD based on the research status and dilemmas of MD. It can be envisioned that MagMem will lead to a paradigm shift in MD, especially by in situ fouling/wetting mitigation and enhancing energy efficiency via in-place actuation and localized heating by MNPs. Moreover, remotely controllable pore tuning and specific or switchable wettability can also be anticipated. Overall, MagMem provides attractive opportunities for advanced robust and efficient MD.

Mixed scaling patterns and mechanisms of high-pressure nanofiltration in hypersaline wastewater desalination.

Nanofiltration (NF) will play a crucial role in salt fractionation and recovery, but the complicated and severe mixed scaling is not yet fully understood. In this work, the mixed scaling patterns and mechanisms of high-pressure NF in zero-liquid discharge (ZLD) scenarios were investigated by disclosing the role of key foulants. The bulk crystallization of CaSO4 and Mg-Si complexes and the resultant pore blocking and cake formation under high pressure were the main scaling mechanisms in hypersaline desalination. The incipient scalants were Mg-Si hydrates, CaF2, CaCO3, and CaMg(CO3)2. Si deposited by adsorption and polymerization prior to and impeded Ca scaling when Mg was not added, thus pore blocking was the main mechanism. The amorphous Mg-Si hydrates contribute to dense cake formation under high hydraulic pressure and permeate drag force, causing rapid flux decline as Mg was added. Humic acid has a high affinity to Ca2+by complexation, which enhances incipient scaling by adsorption or lowers the energy barrier of nucleation but improves the interconnectivity of the foulants layer and inhibits bulk crystallization due to the chelation and directional adsorption. Bovine serum albumin promotes cake formation due to the low electrostatic repulsion and acts as a cement to particles by adsorption and bridging in bulk. This work fills the research gaps in mixed scaling of NF, which is believed to support the application of ZLD and shed light on scaling in hypersaline/ultra-hypersaline wastewater desalination applications.

Impact of Formulation of Photocurable Precursor Mixtures on the Performance and Dimensional Stability of Hierarchical Cation Exchange Membranes.

This work presents a systematic approach to formulating UV curable ionomer coatings that can be used as ion-exchange membranes when they are applied on porous substrates. Ion-exchange membranes fabricated in this way can be a cost-effective alternative to perfluorosulfonic acid membranes, such as Nafion and similar thin ionomer film membranes. Hierarchically structured coated membranes find applications for energy storage and conversion (organic redox flow batteries and artificial photosynthesis cells) and separation processes (electrodialysis). Designing the ionomer precursor for membrane formulation requires the introduction of compounds with drastically different properties into a liquid mixture. Hansen solubility theory was used to find the solvents to compatibilize main formulation components: acrylic sulfone salt (3-sulfopropyl methacrylate potassium salt) and hexafunctional polyester acrylate cross-linker (Ebecryl 830), otherwise nonmiscible or mutely soluble. Among the identified suitable solvents, acrylic acid and acetic acid allowed for optimal mixing of the components and reaching the highest levels of sulfonic group content, providing the desired ion-exchange capacity. Interestingly, they represented a case of a reactive and nonreactive solvent since acrylic acid was built into the ionomer during the UV curing step. Properties of the two membrane variants were compared. Samples fabricated with acetic acid exhibit improved handleability compared with the case of acrylic acid. Acetic acid yielded a lower area-specific resistance (6.4 ± 0.17 Ohm·cm2) compared to acrylic acid (12.1 ± 0.16 Ohm·cm2 in 0.5 M NaCl). This was achieved without severely suppressing the selectivity of the membrane, which was standing at 93.4 and 96.4% for preparation with acetic and acrylic acid, respectively.

When Coordination Polymers Meet Wood: From Molecular Design toward Sustainable Solar Desalination.

Solar-driven interfacial evaporation harnessing solar energy on a water surface provides a sustainable and economic means to efficiently capture freshwater from nontraditional water sources. Endowed with a hierarchical porous structure and mechanical stability, wood-based evaporators represent a renewable alternative to petroleum-based materials. Nonetheless, incidental inferiorities of a low evaporation rate and weak interfacial strength are challenging to overcome. Herein, we propose the usage of chemically stable coordination polymers (Ni-dithiooxamidato, Ni-DTA) as hydrophilic photothermal nanomaterials for the molecular design of robust wood-based evaporators with improved performance. In situ synthesis of Ni-DTA onto the channel wall of balsawood provides sufficient photothermal domains that localize the converted energy for facilitated interfacial evaporation. A rational control of methanol/dimethylformamide ratios enables the coexistence of 1D-nanofibers and 0D-nanoparticles, endowing Balsa-NiDTA with a high evaporation rate of 2.75 kg m-2 h-1 and an energy efficiency of 82% under one-sun illumination. Experimental and simulation results reveal that Ni-DTA polymers with strong hydration ability decrease the equivalent evaporation enthalpy induced by decreased H-bonding density of water molecules near the evaporation interface. The Balsa-NiDTA evaporator showed a high chemical stability, mainly due to the robust Ni-S/Ni-N bonds and the superior cellulose affinity of Ni-DTA. Furthermore, the Balsa-NiDTA evaporator shows an excellent antibacterial activity and low oil-fouling propensity. This work presents a facile and mild strategy to design chemically stable wood-based evaporators, contributing to highly efficient and sustainable solar desalination under harsh conditions.

Towards effective recovery of humate as green fertilizer from landfill leachate concentrate by electro-neutral nanofiltration membrane.

Under the environmental sustainability concept, landfill leachate concentrate can be up-cycled as a useful resource. Practical strategy for effective management of landfill leachate concentrate is to recover the existing humate as fertilizer purpose for plant growth. Herein, we designed an electro-neutral nanofiltration membrane to separate the humate and inorganic salts for achieving a sufficient humate recovery from leachate concentrate. The electro-neutral nanofiltration membrane yielded a high retention of humate (96.54 %) with an extremely low salt rejection (3.47 %), tremendously outperforming the state-of-the-art nanofiltration membranes and exhibiting superior promise in fractionation of humate and inorganic salts. With implementation of the pressure-driven concentration process, the electro-neutral nanofiltration membrane enriched the humate from 1756 to 51,466 mg∙L-1 at a fold of 32.6, enabling 90.0 % humate recovery and 96.4 % desalination efficiency from landfill leachate concentrate. Furthermore, the recovered humate not only exerted no phytotoxicity, but also significantly promoted the metabolism of red bean plants, serving as an effective green fertilizer. The study provides a conceptual and technical platform using high-performance electro-neutral nanofiltration membranes to extract the humate as a promising nutrient for fertilizer application, in view of sustainable landfill leachate concentrate treatment.

Recovery of copper from electroplating sludge using integrated bipolar membrane electrodialysis and electrodeposition.

Electroplating sludge, though a hazardous waste, is a valuable resource as it contains a large amount of precious metals. In this study, copper was recovered from the electroplating sludge using a technology that integrates bipolar membrane electrodialysis (BMED) and electrodeposition. The experimental results showed that Cu2+ in the electroplating sludge was successfully separated and concentrated in the BMED system without adding any chemical reagents; the concentrated Cu2+ was recovered in the form of copper foil in an electrodeposition system. Current density clearly affected the Cu2+ separation and concentration in the BMED system; the current density, solution pH and Cu2+ concentration drastically affected the Cu2+ electrodeposition ratio and the morphology and purity of the obtained copper foil. Under the optimised experimental conditions, 96.4% of Cu2+ was removed from the electroplating sludge and 65.4% of Cu2+ was recovered in the foil form. On increasing the number of electroplating sludge compartments from one to two and three, the current efficiency for recovering Cu2+ increased from 17.4% to 28.5% and 35.2%, respectively, and the specific energy consumption decreased from 11.3 to 6.7 and 5.3 kW h/kg of copper, respectively. The purity of the copper foil was higher than 99.5%. Thus, the integrated technology can be regarded as an effective method for recovering copper from electroplating sludge.

Tailoring properties and performance of thin-film composite membranes by salt additives for water treatment: A critical review.

During the fabrication of thin film composite (TFC) membranes by interfacial polymerization (IP), the utilization of salt additives is one of the effective methods to regulate membrane properties and performance. Despite gradually receiving widespread attention for membrane preparation, the strategies, effects and underlying mechanisms of using salt additives have not yet been systematically summarized. This review for the first time provides an overview of various salt additives used to tailor properties and performance of TFC membranes for water treatment. By classifying salt additives into organic and inorganic salts, the roles of added salt additives in the IP process and the induced changes in membrane structure and properties are discussed in detail, and the different mechanisms of salt additives affecting membrane formation are summarized. Based on these mechanisms, the salt-based regulation strategies have shown great potential for improving the performance and application competitiveness of TFC membranes, including overcoming the trade-off relationship between water permeability and salt selectivity, tailoring membrane pore size distribution for precise solute-solute separation, and enhancing membrane antifouling performance. Finally, future research directions are suggested to focus on the long-term stability assessment of salt-modified membranes, the combined use of different salt additives, and the integration of salt regulation with other membrane design or modification strategies.

Membrane Life Cycle Management: An Exciting Opportunity for Advancing the Sustainability Features of Membrane Separations.

Membrane science and technology is growing rapidly worldwide and continues to play an increasingly important role in diverse fields by offering high separation efficiency with low energy consumption. Membranes have also shown great promise for "green" separation. A majority of the investigations in the field are devoted to the membrane fabrication and modification with the ultimate goals of enhancing the properties and separation performance of membranes. However, less attention has been paid to membrane life cycle management, particularly at the end of service. This is becoming very important, especially taking into account the trends toward sustainable development and carbon neutrality. On the contrary, this can be a great opportunity considering the large variety of membrane processes, especially in terms of the size and capacity of plants in operation. This work aims to highlight the prominent aspects that govern membrane life cycle management with special attention to life cycle assessment (LCA). While fabrication, application, and recycling are the three key aspects of LCA, we focus here on membrane (module) recycling at the end of life by elucidating the relevant aspects, potential criteria, and strategies that effectively contribute to the achievement of green development and sustainability goals.

Nickel recovery from electroplating sludge via bipolar membrane electrodialysis.

In this study, nickel (Ni) was recovered from electroplating sludge in the form of Ni(OH)2 using a bipolar membrane electrodialysis (BMED) system. The results showed that the H+ generated by the bipolar membrane could effectively desorb Ni from the sludge to the solution and the solution pH considerably affected Ni desorption. The desorption process can be described using the first-order kinetic model. The current density and solid/liquid ratio (m/v) considerably affected Ni recovery. Moreover, 100% of Ni was removed from the electroplating sludge and 93.5% of Ni was recovered after 28 h under a current density of 20 mA/cm2, a solid/liquid ratio of 1.0:15 and an electroplating-sludge particle size of 100 mesh. As the number of electroplating compartments increased from one to two and three, the current efficiency for recovering Ni changed from 12.1% to 11.8% and 11.9%, respectively, and the specific energy consumption decreased from 0.064 to 0.048 and 0.039 kW·h/g, respectively. Fourier-transform infrared spectroscopy and Raman spectroscopy showed that the precipitate obtained in this study is similar to commercial Ni(OH)2 and the purity of Ni(OH)2 in the obtained precipitate was 79%. Thus, the results showed that the BMED system is effective for recovering Ni from electroplating sludge.

Recovery of nickel in the form of Ni(OH)2 from plating wastewater containing Ni-EDTA using bipolar membrane electrodialysis.

Ni is often present in plating wastewater as a complexing state. It is difficult to remove this Ni using traditional chemical precipitation technology. In this study, a bipolar membrane electrodialysis system was used to recover Ni in the form of Ni(OH)2 from plating wastewater containing Ni-ethylenediaminetetraacetic acid (Ni-EDTA) without adding chemical reagents. The stable structure of Ni-EDTA can be destroyed by H+ produced by the bipolar membrane to obtain free Ni2+, which can combine with OH- produced by the bipolar membrane to form Ni(OH)2. When the electrolyte Na2SO4 concentration, current density and initial Ni-EDTA concentration were 0.2 mol/L, 16 mA/cm2 and 1000 mg/L, respectively, 99.0% of Ni-EDTA was removed after 32 h. When the system was used to treat actual plating wastewater, 92.1% of Ni-EDTA was removed and 88.7% was recovered. When the number of wastewater compartments in the system was increased from one to three, the current efficiency increased from 1.7% to 5.8%, and the specific energy consumption decreased from 0.39 to 0.19 kW h/g. The results of an X-ray diffraction study indicate that the Ni(OH)2 obtained in this study is similar to commercial Ni(OH)2. Moreover, the recovery mechanism of Ni-EDTA was analysed. Thus, bipolar membrane electrodialysis can be regarded as an effective method to recover Ni from wastewater containing Ni-EDTA.

Advanced Covalent Organic Framework-Based Membranes for Recovery of Ionic Resources.

Membrane technology has shown a viable potential in conversion of liquid-waste or high-salt streams to fresh waters and resources. However, the non-adjustability pore size of traditional membranes limits the application of ion capture due to their low selectivity for target ions. Recently, covalent organic frameworks (COFs) have become a promising candidate for construction of advanced ion separation membranes for ion resource recovery due to their low density, large surface area, tunable channel structure, and tailored functionality. This tutorial review aims to analyze and summarize the progress in understanding ion capture mechanisms, preparation processes, and applications of COF-based membranes. First, the design principles for target ion selectivity are illustrated in terms of theoretical simulation of ions transport in COFs, and key properties for ion selectivity of COFs and COF-based membranes. Next, the fabrication methods of diverse COF-based membranes are classified into pure COF membranes, COF continuous membranes, and COF mixed matrix membranes. Finally, current applications of COF-based membranes are highlighted: desalination, extraction, removal of toxic metal ions, radionuclides and lithium, and acid recovery. This review presents promising approaches for design, preparation, and application of COF-based membranes in ion selectivity for recovery of ionic resources.

Intensification of Middle- and High-Molecular-Weight Toxins Removal in Dialysis Process.

A novel extracorporeal circuit for hemodialysis is described, which enhances the removal of middle- and high-molecular-weight toxins. To enhance the removal of especially high-molecular toxins, a recirculation pathway for dialysate flow is added to conventional circuit. The influence of an increase in the ratio of recirculation to dialysate flow rate and the ultrafiltration rate (UFR) on the removal of toxins was investigated to evaluate the removal of different toxins in clinical conditions. Removal of toxins was also modeled by an analytical method and solved by the MATLAB software (The MathWorks, Inc., Natick, MA). A significant increase in removal of urea (up to 31%) and vitamin B12 (11%) was achieved when the UFR is low (≤50 ml/h) or zero. The model showed an excellent agreement with the experimental results, which indicates its applicability for the removal of different toxins in an extracorporeal circuit. Increase in recirculation flow, while adjusting the UFR near zero, improves the mass transfer coefficient and can lead to enhanced especially middle- and high-molecular-weight toxin removal.

Ionic resource recovery for carbon neutral papermaking wastewater reclamation by a chemical self-sufficiency zero liquid discharge system.

Papermaking industry discharges large quantities of wastewater and waste gas, whose treatment is limited by extra chemicals requirements, insufficient resource recovery and high energy consumption. Herein, a chemical self-sufficiency zero liquid discharge (ZLD) system, which integrates nanofiltration, bipolar membrane electrodialysis and membrane contactor (NF-BMED-MC), is designed for the resource recovery from wastewater and waste gas. The key features of this system include: 1) recovery of NaCl from pretreated papermaking wastewater by NF, 2) HCl/NaOH generation and fresh water recovery by BMED, and 3) CO2 capture and NaOH/Na2CO3 generation by MC. This integrated system shows great synergy. By precipitating hardness ions in papermaking wastewater and NF concentrate with NaOH/Na2CO3, the inorganic scaling on NF membrane is mitigated. Moreover, the NF-BMED-MC system with high stability can simultaneously achieve efficient CO2 removal and sustainable recovery of fresh water and high-purity resources (NaCl, Na2SO4, NaOH and HCl) from wastewater and waste gas without introducing any extra chemicals. The environmental evaluation indicates the carbon-neutral papermaking wastewater reclamation can be achieved through the application of NF-BMED-MC system. This study establishes the promising of NF-BMED-MC as a sustainable alternative to current membrane methods for ZLD of papermaking industry discharges treatment.