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Reverse osmosis (RO) is affected by multiple types of fouling such as biofouling, scaling, and organic fouling. Therefore, a multi-functional membrane capable of reducing more than one type of fouling is a need of the hour. The polyacrylic acid and graphene oxide (PAA-GO) nanocomposite functionalization of the RO membrane has shown its effectiveness against both mineral scaling and biofouling. In this research, the polyacrylic acid concentration and irradiation times were optimized for the PAA-GO-coated RO membrane using the response surface methodology (RSM) approach. The effect of these parameters on pure water permeability and salt rejection was investigated. The models were developed through the design of the experiment (DoE), which were further validated through the analysis of variance (ANOVA). The optimum conditions were found to be: 11.41 mg·L−1 (acrylic acid concentration) and 28.08 min (UV activation times) with the predicted results of 2.12 LMH·bar−1 and 98.5% NaCl rejection. The optimized membrane was prepared as per the model conditions, which showed an increase in both pure water permeability and salt rejection as compared to the control. The improvement in membrane surface smoothness and hydrophilicity for the optimized membrane also helped to inhibit mineral scaling by 98%. [ABSTRACT FROM AUTHOR]

In this paper, novel composite materials from modified roasted date pits using ferrocyanides were developed and investigated for the recovery of lithium ions (Li+) from seawater reverse osmosis (RO) brine. Two composite materials were prepared from roasted date pits (RDP) as supporting material, namely potassium copper hexacyanoferrate-date pits composite (RDP-FC-Cu), and potassium nickel hexacyanoferrate-date pits composite (RDP-FC-Ni). The physiochemical characterization of the RO brine revealed that it contained a variety of metals and salts such as strontium, zinc, lithium, and sodium chlorides. RDP-FC-Cu and RDP-FC-Ni exhibited enhanced chemical and physical characteristics than RDP. The optimum pH, which attained the highest adsorption removal (%) for all adsorbents, was at pH 6. In addition, the highest adsorption capacities for the adsorbents were observed at the initial lithium concentration of 100 mg/L. The BET surface area analysis confirmed the increase in the total surface area of the prepared composites from 2.518 m2/g for RDP to 4.758 m2/g for RDP-FC-Cu and 5.262 m2/g for RDP-FC-Ni. A strong sharp infrared peak appeared for the RDP-FC-Cu and RDP-FC-Ni at 2078 cm−1. This peak corresponds to the C≡N bond, which indicates the presence of potassium hexacyanoferrate, K4[Fe(CN)6]. The adsorption removal of lithium at a variety of pH ranges was the highest for RDP-FC-Cu followed by RDP-FC-Ni and RDP. The continuous increase in the adsorption capacity for lithium with increasing initial lithium concentrations was also observed. This could be mainly attributed to enhance and increased lithium mass transfer onto the available adsorption active sites on the adsorbents' surface. The differences in the adsorption in terms of percent adsorption removal were clear and significant between the three adsorbents (P value < 0.05). All adsorbents in the study showed a high lithium desorption percentage as high as 99%. Both composites achieved full recoveries of lithium from the RO brine sample despite the presence of various other competing ions. [ABSTRACT FROM AUTHOR]

This study aims to prepare an ion-imprinted polymer (IIP) using copper sulfate as a template and potassium persulfate as an initiator to selectively adsorb copper ions (Cu2+) from aqueous solutions and in an attempt to also test its applicability for removing strontium ions (Sr2+). The prepared polymer was denoted by IIP-Cu. Various physical and chemical characterizations were performed for the prepared IIP-Cu. The scanning electron microscopy and transmission electron microscopy analyses confirmed the cavities formed after the removal of the template. It also indicated that the IIP-Cu had a rough and porous topology. The X-ray photoelectron spectroscopy confirmed the successful removal of the Cu template from IIP-Cu. The Brunauer-Emmet-Teller revealed that the surface area of IIP-Cu is as high as 152.3 m2/g while the pore radius is 8.51 nm. The effect of pH indicated that the maximum adsorption of Cu2+ was achieved at pH 8 with 98.7%. Isotherm studies revealed that the adsorption of Cu2+ was best explained using Langmuir models with a maximum adsorption capacity of 159 mg/g. The effect of temperature revealed that an increase in temperature had an adverse impact on Cu2+ removal from the aqueous solution, which was further confirmed by thermodynamic studies. The negative value of standard enthalpy change (−4.641 kJ/mol) revealed that the adsorption of Cu2+ onto IIP-Cu was exothermic. While the continuous increase in Gibbs free energy from −6776 kJ/mol to −8385 kJ/mol with the increase in temperature indicated that the adsorption process was spontaneous and feasible. Lastly, the positive value of the standard entropy change (0.023 J/mol.K) suggested that the Cu2+ adsorption onto IIP-Cu had a good affinity at the solid-liquid surface. The efficiency of the prepared IIP-Cu was also tested by studying the adsorption capacity using Sr2+ and real brine water. The results revealed that IIP-Cu was able to remove 63.57% of Sr2+ at pH 8. While the adsorption studies revealed that the experiment was best described using the Langmuir model with a maximum adsorption capacity of 76.92 mg/g. Additionally, IIP-Cu was applied in a real brine sample, which consisted of various metal ions. The highest percentage of Cu2+ removal was 90.6% and the lowest was 65.63% in 1:4 and 1:1 brine ratios, respectively. However, this study indicates the successful application of IIP-Cu in a real sample when it comes to the effective and efficient removal of Cu2+ in a solution consisting of various competing ions. • IIP-Cu was successfully fabricated using potassium persulfate as an initiator. • The prepared IIP-Cu demonstrated high affinity and selectivity towards Cu2+. • The maximum removal of 98.7% Cu2+ and 63.57%.Sr2+ was achieved at pH 8. • High desorption efficiencies for both Cu2+ and Sr2+ were achieved. • IIP-Cu showed excellent removal removals 90.6% Cu2+ and 82.6% Sr2+ from real brine. [ABSTRACT FROM AUTHOR]

Pesticides are used in agriculture to protect crops from pathogens, insects, fungi and weeds, but the release of pesticides into surface/groundwater by agriculture runoff and rain has raised serious concerns not only for the environment but also for human health. This study aimed to investigate the impact of surface properties on the performance of seven distinct membrane types utilized in nanofiltration (NF), reverse osmosis (RO) and forward osmosis (FO) processes in eliminating multiple pesticides from spiked water. Out of the membranes tested, two are self-fabricated RO membranes while the rest are commercially available membranes. Our results revealed that the self-fabricated RO membranes performed better than other commercial membranes (e.g., SW30XLE, NF270, Duracid and FO) in rejecting the targeted pesticides by achieving at least 99% rejections regardless of the size of pesticides and their log K ow value. Despite the marginally lower water flux exhibited by the self-fabricated membrane compared to the commercial BW30 membrane, its exceptional ability to reject both mono- and divalent salts renders it more apt for treating water sources containing not only pesticides but also various dissolved ions. The enhanced performance of the self-fabricated RO membrane is mainly attributed to the presence of a hydrophilic interlayer (between the polyamide layer and substrate) and the incorporation of hydrophilic nanosheets in tuning its surface characteristics. The findings of the work provide insight into the importance of membrane surface modification for the application of not only the desalination process but also for the removal of contaminants of emerging concern. [Display omitted] • Membrane rejection against pesticides varied depending on its physiochemical properties. • RO membranes showed the highest pesticides rejection followed by NF and FO membranes. • Improving surface properties of RO membranes using GO further enhanced pesticides removal. • GO-modified RO membrane achieved >99% rejections regardless of pesticide size and log K ow. [ABSTRACT FROM AUTHOR]

In this study, three types of adsorbents were used to remove and recover strontium ions (Sr2+) from aqueous and brine solution of seawater reverse osmosis (SWRO), namely roasted date pits (RDP) and RDP modified using copper and nickel salts of potassium hexacyanoferrates to obtain RDP–FC–Cu, and RDP–FC–Ni, respectively. Additionally, the influence of various parameters, including pH, temperature, initial concentration, and co-existing ions was also evaluated. The results revealed that pH 10 was the optimum pH in which the maximum Sr2+ ions were adsorbed. Additionally, all adsorbents had a high adsorption capacity (99.9 mg/g) for removing Sr2+ ions at the highest concentration (100 mg/L) and a temperature of 45 °C was found to be the optimum temperature. A scanning electron microscopy for the adsorbents before and after the adsorption of strontium showed the remarkable pore filling onto the active sites of all adsorbents. The thermodynamics parameter demonstrated that the adsorption occurred in an endothermic environment, and that, the reaction was spontaneous, and favorable at all the temperatures investigated. According to isotherm studies, the Langmuir model was the best-fit isotherm model; indicating that strontium adsorption involved the formation of monolayers and multilayers at higher temperatures (45 °C). Furthermore, high desorption percentages (above 90%) were achieved for all the adsorbents when an HCl concentration of 0.5 M was used. This showed the high reusability of the adsorbents. Lastly, the adsorption of strontium from the SWRO brine containing a number of metal ions was extremely sufficient as all the adsorbents were efficient to adsorb a high amount of Sr2+ despite the presence of other competing ions. [Display omitted] • Three adsorbents were investigated to remove and recover strontium ions (Sr2+) from brine solution. • PH 6 was the optimum pH in which the maximum Sr2+ was adsorbed. • 99.9 mg/g adsorption capacity was achieved for all adsorbents at the concentration of 100 mg Sr2+/L and 45 °C. • >90% desorption percentages were achieved for all the adsorbents at 0.5 M HCl. [ABSTRACT FROM AUTHOR]

This study examines which management methods are the most recent and advanced in managing rejected brine generated from desalination plants. It also provides up-to-date information regarding the most adequate technologies that generate a minimum quantity of rejected brine via the use of minimization techniques and analyzes the method of direct disposal that has lately received noticeable improvements. It further discusses the reuse of discarded brine to recover valuable goods and sequestration of carbon dioxide. Sustainability is an important parameter that needs consideration to achieve uninterrupted operation of the discarded brine management to achieve the least environmental, social, and economic aftermath. To properly deal with any environmental issues related to brine disposal, different methods are implemented so that, in the end, higher water recovery is achievable from the desalination processes, namely brine minimization and rejection technologies (pressure retarded osmosis, microbial desalination cell technology), membrane-based technologies (vibratory shear enhanced processing, forward osmosis, electrodialysis, electrodialysis reverse, and electrodialysis metathesis, pervaporation method, thermal-based technologies (wind-aided intensified evaporation, brine concentrators, ohmic evaporator, membrane distillation, multi-stage flash distillation. This review also critically examined the two conventional approaches commonly used in life cycle assessment (LCA), when evaluating the ecotoxic effect of discarded brine. It intends to discuss the currently available methods and propose an improved method for evaluating the toxicity potential of brine on the aquatic ecosystem originated from seawater desalination plants. The Group-by-Group method takes into consideration the demerits of the two methods of the traditional method of LCA or chemical-specific approach as it provides a more holistic coverage for complicated brine to be disposed of. Recently, attention has been focused on recovering valuable metals from the discharged concentrated brine waste. Certainly, attaining marketable products from the discharged concentrated brine would offer an economic benefit and reducing the whole desalination costs. Ion imprinting polymers have potential applications in metal recovery from brine. Finding selective, more efficient, and less expensive imprinted polymers for extraction/pre-concentration of valuable ions is a vital and challenging task. Lastly, the brine should be seen as a resource and not as a waste to attain sustainability in its management approaches. Hybrid processes would be highly recommended to get the absolute transformation of the discarded brine from desalination processes to more valuable constituents. [Display omitted] • Brine is best managed when reducing its volume to the bare and accepted levels. • Brine is considered as a resource to achieve sustainability in water management. • All the emerging technologies are suitable for minimizing the brine volume. • The "group-by-group" approach can evaluate the ecotoxic effect of discarded brine. • Ion imprinting polymers have potential applications in metal recovery from brine. [ABSTRACT FROM AUTHOR]