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As a type of gas that contributes to air pollution, nitrogen oxide (NOx) has harmful effects on humans and the environment. Among several types of NOx, nitric oxide (NO) and nitrogen dioxide (NO2) are most commonly found in air. The utilization of membranes as reactors is a system that combines chemical reactions with the separation process through membranes to increase the conversion of the reaction. This study investigated the absorption process by utilizing a hollow fiber membrane module (polysulfone) as a bubble reactor with H2O2 (0.5 wt.%) and HNO3 (0.5M) as the absorbent. NOx feed gas was flown into the tube side of the membrane; the shell side was filled with static H2O2 and HNO3 and the shell input and the tube output flow were closed to create gas bubbles. The experimental results showed that the absorption efficiency increased, but the mass transfer coefficient and flux decreased as the number of fibers in the membrane module increased at the same feed gas flow rate. The NOx loading is relatively constant as the amount of fiber in the membrane module increased at the same feed gas flow rate. The experimental results also showed that the mass transfer coefficient, flux, and NOx loading increased with increasing feed gas flow rate, but the absorption efficiency decreased when using the same number of fibers in the membrane module. The maximum NOx absorption efficiency achieved in this study was 94.6% at the feed gas flow rate of 0.1 L/min, using a membrane module with 48 fibers.

The increase in the global population has caused an increment in energy demand, and therefore, energy production has to be maximized through various means including the burning of natural gas. However, the purification of natural gas has caused CO2 levels to increase. Hollow fiber membranes offer advantages over other carbon capture technologies mainly due to their large surface-to-volume ratio, smaller footprint, and higher energy efficiency. In this work, hollow fiber mixed matrix membranes (HFMMMs) were fabricated by utilizing cellulose triacetate (CTA) as the polymer and amine-functionalized metal-organic framework (NH2-MIL-125(Ti)) as the filler for CO2 and CH4 gas permeation. CTA and NH2-MIL-125(Ti) are known for exhibiting a high affinity towards CO2. In addition, the utilization of these components as membrane materials for CO2 and CH4 gas permeation is hardly found in the literature. In this work, NH2-MIL-125(Ti)/CTA HFMMMs were spun by varying the air gap ranging from 1 cm to 7 cm. The filler dispersion, crystallinity, and functional groups of the fabricated HFMMMs were examined using EDX mapping, SEM, XRD, and FTIR. From the gas permeation testing, it was found that the NH2-MIL-125(Ti)/CTA HFMMM spun at an air gap of 1 cm demonstrated a CO2/CH4 ideal gas selectivity of 6.87 and a CO2 permeability of 26.46 GPU.

Abstract Carbon dioxide (CO2) is responsible for increment of the Earth surface temperature and the subsequent environmental issues. In this regard, membrane contactor is one of the emerging technologies that can be applied for controlling CO2 emission. More specifically, the intrinsic structure of membrane plays an important role to govern the performance of CO2 absorption. In this study, considering stretching ratio (SR) as a key factor to affect membrane structural properties, highly porous poly(vinylidene fluoride-co-hexafluoropropylene) (PVDF-HFP) hollow fiber membranes were fabricated by a non-solvent induced phase separation method. The results showed that the membrane dimension and thickness were significantly reduced by optimizing the SR. The optimum membrane structure was found at SR of 1.5 where the mean pore size, CO2 permeance, collapsing pressure and liquid entry pressure of 0.032 μm, 3440 GPU, 550 kPa and 500 kPa were achieved, respectively. The prepared membranes showed open structure with overall porosity of more than 80%. The upgraded membrane at SR of 1.5 presented the maximum CO2 absorption flux of 9.8 × 10− 4 mol/m2 s and the minimum mass transfer resistance of 49,544 (m/s)−1. Furthermore, a stable CO2 absorption performance was achieved during 80 h continuous operation with a flux decline of only about 9%. The findings of this work demonstrated that by applying a cost-effective fabrication method, we can potentially enhance the PVDF-HFP membrane properties for CO2 adsorption without requiring an additional post-modification step.

Introduction: Nanomaterials aggregation within polyamide (PA) layer of thin film nanocomposite (TFN) membrane is found to be a common issue and can negatively affect membrane filtration performance. Thus, post-treatment on the surface of TFN membrane is one of the strategies to address the problem. Objective: In this study, an eco-friendly surface modification technique based on plasma enhanced chemical vapour deposition (PECVD) was used to deposit hydrophilic acrylic acid (AA) onto the PA surface of TFN membrane with the aims of simultaneously minimizing the PA surface defects caused by nanomaterials incorporation and improving the membrane surface hydrophilicity for reverse osmosis (RO) application. Methods: The TFN membrane was first synthesized by incorporating 0.05 wt% of functionalized titania nanotubes (TNTs) into its PA layer. It was then subjected to 15-s plasma deposition of AA monomer to establish extremely thin hydrophilic layer atop PA nanocomposite layer. PECVD is a promising surface modification method as it offers rapid and solvent-free functionalization for the membranes. Results: The findings clearly showed that the sodium chloride rejection of the plasma-modified TFN membrane was improved with salt passage reduced from 2.43% to 1.50% without significantly altering pure water flux. The AA-modified TFN membrane also exhibited a remarkable antifouling property with higher flux recovery rate (>95%, 5-h filtration using 1000 mg/L sodium alginate solution) compared to the unmodified TFN membrane (85.8%), which is mainly attributed to its enhanced hydrophilicity and smoother surface. Furthermore, the AA-modified TFN membrane also showed higher performance stability throughout 12-h filtration period. Conclusion: The deposition of hydrophilic material on the TFN membrane surface via eco-friendly method is potential to develop a defect-free TFN membrane with enhanced fouling resistance for improved desalination process.

Ammonium is known to be one of the most significant pollutants in water bodies. The presence of ammonium in water is mainly originated from agricultural activities, domestic sewage and industrial effluent. This study evaluates the performance of two commercial thin film composite (TFC) membranes, i.e., NF270 and XLE from FilmTec™ for ammonium removal using synthetic wastewater and domestic sewage. The filtration experiment was conducted at different feed ammonium concentrations, humic acid concentrations, pHs and pressure. Results showed that the membrane rejection against ammonium increased dramatically with increasing ammonium concentration. However, the membrane flux was slightly compromised at higher ammonium concentration. With respect to pH, highest ammonium removal rate was able to be achieved at an optimum pH of 10. Besides, the permeation flux increased gradually with increasing feed pressure. From the results, the XLE membrane outperformed the NF270 membrane in terms of ammonium rejection. The retentate of XLE membrane filtration process was found to be useful as liquid fertiliser for plant growth. The results indicated that the TFC membrane process is not only able to produce permeate with an ammonium concentration below the acceptable limit of 10 mg/L but also able to produce retentate with enriched ammonium for plant growth.

The presence of ciprofloxacin (CIP) and ampicillin (AMP) as emerging contaminant in water is a serious global challenge requiring affordable and sustainable solution. In response to this, this study prepared a mixed metal oxide, zinc oxide (ZnO)-magnesium oxide (MgO)-nickel oxide (NiO)@stearicamide for the removal of CIP and AMP from aqueous solution. The properties of ZnO-MgO-NiO@Stearicamide were confirmed with several analyses including Fourier transformed infrared spectroscopy (FTIR), Brunauer-Emmett-Teller (BET), transmission electron microscopy (TEM), X-ray diffraction (XRD) and energy-dispersive X-ray spectroscopy (EDX). ZnO-MgO-NiO@Stearicamide has a BET surface area of 13.50 m2 g−1 and an average particle size of 12.50 nm. The sorption of CIP and AMP from solution by ZnO-MgO-NiO@Stearicamide showed a removal of 83.87 % and 81.10 %, respectively in a process that can be described by the Langmuir isotherm and electrostatic interaction. The sorption process has enthalpy (ΔH), entropy (ΔS) and free energy change (ΔG) which suggests the process to be spontaneous and exothermic. It is also found that synthesized metal mixed oxide could maintain a regeneration capacity that is > 80 % even after 11th regeneration cycle. The experimental findings indicate that the self-synthesized ZnO-NiO-MgO@Stearicamide is a potential material to treat CIP- and AMP-contaminated water source.

Most researchers focused on developing highly selective membranes for CO2/CH4 separation, but their developed membranes often suffered from low permeance. In this present work, we aimed to develop an ultrahigh permeance membrane using a simple coating technique to overcome the trade-off between membrane permeance and selectivity. A commercial silicone membrane with superior permeance but low CO2/CH4 selectivity (in the range of 2–3) was selected as the host for surface modification. Our results revealed that out of the three silane agents tested, only tetraethyl orthosilicate (TEOS) improved the control membrane’s permeance and selectivity. This can be due to its short structural chain and better compatibility with the silicone substrate. Further investigation revealed that higher CO2 permeance and selectivity could be attained by coating the membrane with two layers of TEOS. The surface integrity of the TEOS-coated membrane was further improved when an additional polyether block amide (Pebax) layer was established atop the TEOS layer. This additional layer sealed the pin holes of the TEOS layer and enhanced the resultant membrane’s performance, achieving CO2/CH4 selectivity of ~19 at CO2 permeance of ~2.3 × 105 barrer. This performance placed our developed membrane to surpass the 2008 Robeson Upper Boundary.

In this current study, facile, one-pot synthesis of functionalised nanocomposite coating with simultaneous hydrophilic and oleophobic properties was successfully achieved via the sol–gel technique. The synthesis of this nanocomposite coating aims to develop a highly efficient, simultaneously oleophobic-hydrophilic coating intended for polymer membranes to spontaneously separate oil-in-water emulsions, therefore, mitigating the fouling issue posed by an unmodified polymer membrane. The simultaneous hydrophilicity-oleophobicity of the nanocoating can be applied onto an existing membrane to improve their capability to spontaneously separate oil-in-water substances in the treatment of oily wastewater using little to no energy and being environmentally friendly. The synthesis of hybrid chitosan–silica (CTS-Si)/halloysite nanotube (HNT) nanocomposite coating using the sol–gel method was presented, and the resultant coating was characterised using FTIR, XPS, XRD, NMR, BET, Zeta Potential, and TGA. The wettability of the nanocomposite coating was evaluated in terms of water and oil contact angle, in which it was coated onto a polymer substrate. The coating was optimised in terms of oil and water contact angle using Response Surface Modification (RSM) with Central Composite Design (CCD) theory. The XPS results revealed the successful grafting of organosilanes groups of HNT onto the CTS-Si denoted by a wide band between 102.6–103.7 eV at Si2p. FTIR spectrum presented significant peaks at 3621 cm−1; 1013 cm−1 was attributed to chitosan, and 787 cm−1 signified the stretching of Si-O-Si on HNT. 29Si, 27Al, and 13H NMR spectroscopy confirmed the extensive modification of the particle’s shells with chitosan–silica hybrid covalently linked to the halloysite nanotube domains. The morphological analysis via FESEM resulted in the surface morphology that indicates improved wettability of the nanocomposite. The resultant colloids have a high colloid stability of 19.3 mV and electrophoretic mobility of 0.1904 µmcm/Vs. The coating recorded high hydrophilicity with amplified oleophobic properties depicted by a low water contact angle (WCA) of 11° and high oil contact angle (OCA) of 171.3°. The optimisation results via RSM suggested that the optimised sol pH and nanoparticle loadings were pH 7.0 and 1.05 wt%, respectively, yielding 95% desirability for high oil contact angle and low water contact angle.

NOx (NO and NO2) are air toxins that endanger life and represent a hazard to the environment, such as photochemical smog, global warming, acid rain, ozone depletion, and the occurrence of respiratory infections. Some technological strategies to diminish NOx emissions to meet regulations depend on two techniques: the dry process and the wet process. This study applies polyvinylidene fluoride (PVDF) hollow fiber membrane modules as a medium to remove NOx from solutions containing several absorbents such as hydrogen peroxide and nitric acid (H2O2-HNO3) solutions, sodium chlorite and sodium hydroxide (NaClO2-NaOH) solutions, and sodium chlorate and sodium hydroxide (NaClO3-NaOH) solutions. The experimental results showed that the oxidant’s strength influences NOx removal efficiency, where the absorbent solutions containing hydrogen peroxide had the highest removal efficiency as hydrogen peroxide is the most potent oxidant, followed by sodium chlorite and sodium chlorate. The three pairs of absorbents also gave a high NOx removal efficiency (above 90%), which means that all the absorbents used in the study are very potential to be used to diminish NOx via the wet process. NOx removal efficiency at the same feed gas flow rate increased as the number of fiber and absorbent concentrations is increased. However, NOx removal efficiency is reduced as the feed gas flow rate is increased at the same membrane module and absorbent concentration.

The effects of flipping membranes with hydrophilic/hydrophobic asymmetry are well documented in the literature, but not much is known on the impact of flipping a membrane with dense/porous layer asymmetry. In this work, the pure water flux (PWF) of a commercial polyethersulfone (PES) membrane and a ceramic ultrafiltration (UF) membrane was measured in the normal and inverted positions. Our experimental results showed that the PWF was two orders of magnitude higher when the PES membrane was flipped to the inverted position, while the increase was only two times for the ceramic membrane. The filtration experiments were also carried out using solutions of bovine serum albumin and poly(vinylpyrrolidone). A mathematical model was further developed to explain the PWF increase in the inverted position based on the Bernoulli’s rule, considering a straight cylindrical pore of small radius connected to a pore of larger radius in series. It was found by simulation that a PWF increase was indeed possible when the solid ceramic membrane was flipped, maintaining its pore geometry. The flow from a layer with larger pore size to a layer with smaller pore size occurred in the backwashing of the fouled membrane and in forward and pressure-retarded osmosis when the membrane was used with its active layer facing the draw solution (AL-DS). Therefore, this work is of practical significance for the cases where the direction of the water flow is in the inverted position of the membrane.

Fulfilling the demand of clean potable water to the general public has long been a challenging task in most developing countries due to various reasons. Large-scale membrane water treatment systems have proven to be successful in many advanced countries in the past two decades. This paves the way for developing countries to study the feasibility and adopt the utilization of membrane technology in water treatment. There are still many challenges to overcome, particularly on the much higher capital and operational cost of membrane technology compared to the conventional water treatment system. This review aims to delve into the progress of membrane technology for water treatment systems, particularly in developing countries. It first concentrates on membrane classification and its application in water treatment, including membrane technology progress for large-scale water treatment systems. Then, the fouling issue and ways to mitigate the fouling will be discussed. The feasibility of membrane technologies in developing countries was then evaluated, followed by a discussion on the challenges and opportunities of the membrane technology implementation. Finally, the current trend of membrane research was highlighted to address future perspectives of the membrane technologies for clean water production.

Air pollution has become a global issue and contributes significantly to climate change, mainly due to the massive energy consumption in industry and the transportation sector. Emissions of harmful gases from burning fuels such as NOx and SO2 are the most significant sources of environmental pollution, which have negative impacts on the environment, such as the greenhouse effect, damage to the ozone layer, photochemical smog, and acid rain, and can interfere with the respiratory system in humans. This study utilizes hollow fiber membrane modules, which act as a reactor on the shell side of the membrane module and a gas distributor by the membrane fiber to remove NOx and SO2 spontaneously. The oxidant solutions used were a pair of hydrogen peroxide and sodium hydroxide (H2O2-NaOH) solutions, a pair of sodium chlorite and sodium hydroxide (NaClO2-NaOH) solutions, and a pair of sodium chlorate and sodium hydroxide (NaClO3-NaOH) solutions. Based on the results of experiments, SO2 can be removed entirely in the process, while NOx depends on the feed gas flow rate and the concentration of the oxidant solution used. H2O2 is the most effective oxidizing agent in removing NOx and SO2 because of its higher oxidative properties than NaCLO2 and NaClO3. The increase in feed gas flow rate resulted in a decrease in the efficiency of NOx removal even though the NOx mass transfer flux and NOx loading increased. Meanwhile, an increase in the concentration of oxidants increases the efficiency of NOx removal and mass transfer flux but decreases NOx loading. Based on the experimental results, the maximum NOx removal efficiency achieved by the oxidant solutions is 93.9, 91.1, and 88.3% for H2O2-NaOH, NaClO2-NaOH, and NaClO3-NaOH, respectively. [ABSTRACT FROM AUTHOR]

Dialyzers have been commercially used for hemodialysis application since the 1950s, but progress in improving their efficiencies has never stopped over the decades. This article aims to provide an up-to-date review on the commercial developments and recent laboratory research of dialyzers for hemodialysis application and to discuss the technical aspects of dialyzer development, including hollow fiber membrane materials, dialyzer design, sterilization processes and flow simulation. The technical challenges of dialyzers are also highlighted in this review, which discusses the research areas that need to be prioritized to further improve the properties of dialyzers, such as flux, biocompatibility, flow distribution and urea clearance rate. We hope this review article can provide insights to researchers in developing/designing an ideal dialyzer that can bring the best hemodialysis treatment outcomes to kidney disease patients.

Abstract Despite its attractive features for energy saving separation, the performance of forward osmosis (FO) has been restricted by internal concentration polarization and fast fouling propensity that occur in the membrane sublayer. These problems have significantly affected the membrane performance when treating highly contaminated oily wastewater. In this study, a novel double-skinned FO membrane with excellent anti-fouling properties has been developed for emulsified oil-water treatment. The double-skinned FO membrane comprises a fully porous sublayer sandwiched between a highly dense polyamide (PA) layer for salt rejection and a fairly loose dense bottom zwitterionic layer for emulsified oil particle removal. The top dense PA layer was synthesized via interfacial polymerization meanwhile the bottom layer was made up of a zwitterionic polyelectrolyte brush - (poly(3-(N-2-methacryloxyethyl-N,N-dimethyl) ammonatopropanesultone), abbreviated as PMAPS layer. The resultant double-skinned membrane exhibited a high water flux of 13.7 ± 0.3 L/m2.h and reverse salt transport of 1.6 ± 0.2 g/m2.h under FO mode using 2 M NaCl as the draw solution and emulsified oily solution as the feed. The double-skinned membrane outperforms the single-skinned membrane with much lower fouling propensity for emulsified oil-water separation.

The structural (S) parameter of a medium is used to represent the mass transport resistance of an asymmetric membrane. In this study, we aimed to fabricate a membrane sublayer using a novel composition to improve the S parameter for enhanced forward osmosis (FO). Thin film composite (TFC) membranes using polyamide (PA) as an active layer and different polysulfone:polyethersulfone (PSf:PES) supports as sublayers were prepared via the phase inversion technique, followed by interfacial polymerization. The membrane made with a PSf:PES ratio of 2:3 was observed to have the lowest contact angle (CA) with the highest overall porosity. It also had the highest water permeability (A; 3.79 ± 1.06 L m−2 h−1 bar−1) and salt permeability (B; 8.42 ± 2.34 g m−2 h−1), as well as a good NaCl rejection rate of 74%. An increase in porosity at elevated temperatures from 30 to 40 °C decreased Sint from 184 ± 4 to 159 ± 2 μm. At elevated temperatures, significant increases in the water flux from 13.81 to 42.86 L m−2 h−1 and reverse salt flux (RSF) from 12.74 to 460 g m−2 h−1 occur, reducing Seff from 152 ± 26 to 120 ± 14 μm. Sint is a temperature-dependent parameter, whereas Seff can only be reduced in a high-water- permeability membrane at elevated temperatures.

Water constitutes one of the basic necessities of life. Around 71% of the Earth is covered by water, however, not all of it is readily available as fresh water for daily consumption. Fresh water scarcity is a chronic issue which poses a threat to all living things on Earth. Seawater, as a natural resource abundantly available all around the world, is a potential water source to fulfil the increasing water demand. Climate-independent seawater desalination has been touted as a crucial alternative to provide fresh water. While the membrane-based desalination process continues to dominate the global desalination market, the currently employed membrane fabrication materials and processes inevitably bring adverse impacts to the environment. This review aims to elucidate and provide a comprehensive outlook of the recent efforts based on greener approaches used for desalination membrane fabrication, which paves the way towards achieving sustainable and eco-friendly processes. Membrane fabrication using green chemistry effectively minimizes the generation of hazardous compounds during membrane preparation. The future trends and recommendations which could potentially be beneficial for researchers in this field are also highlighted.

Polymeric membrane is susceptible to fouling particularly when it is used to treat surface water contaminated by natural organic matters and bacteria. Surface modification may address the issue by imparting antifouling and antibacterial properties to the membrane. In this study, a neat polyethersulfone (PES) membrane (denoted as membrane P1) was prepared by phase inversion method followed by polydopamine (PDA) coating to improve its membrane hydrophilicity. Thereafter, the physicochemical properties of the PDA-coated PES membrane (denoted as membrane P3) were further improved by in situ reduction of silver (Ag) onto its surface to impart antibacterial properties (denoted as membrane P4). All membranes were instrumentally characterized while their filtration performance against humic acid (HA) and antibacterial properties were evaluated. Results showed that membrane P1 removed 77.81% of HA and achieved a fouling recovery rate (FRR) of 65.72%. Upon Ag immobilization, the HA rejection of membrane P4 was further improved to 95.14% with FRR recorded at 92.17%. This membrane also demonstrated good stability and excellent antibacterial properties over other fabricated membranes (P1, P2 and P3) in this study. Moreover, it exhibited a lower total flux decline and higher contaminant removal performance over membrane P1 in treating surface water samples. [ABSTRACT FROM AUTHOR]

In this work, several ultrafiltration (UF) membranes with enhanced antifouling properties were fabricated using a rapid and green surface modification method that was based on the plasma-enhanced chemical vapor deposition (PECVD). Two types of hydrophilic monomers—acrylic acid (AA) and 2-hydroxyethyl methacrylate (HEMA) were, respectively, deposited on the surface of a commercial UF membrane and the effects of plasma deposition time (i.e., 15 s, 30 s, 60 s, and 90 s) on the surface properties of the membrane were investigated. The modified membranes were then subjected to filtration using 2000 mg/L pepsin and bovine serum albumin (BSA) solutions as feed. Microscopic and spectroscopic analyses confirmed the successful deposition of AA and HEMA on the membrane surface and the decrease in water contact angle with increasing plasma deposition time strongly indicated the increase in surface hydrophilicity due to the considerable enrichment of the hydrophilic segment of AA and HEMA on the membrane surface. However, a prolonged plasma deposition time (>15 s) should be avoided as it led to the formation of a thicker coating layer that significantly reduced the membrane pure water flux with no significant change in the solute rejection rate. Upon 15-s plasma deposition, the AA-modified membrane recorded the pepsin and BSA rejections of 83.9% and 97.5%, respectively, while the HEMA-modified membrane rejected at least 98.5% for both pepsin and BSA. Compared to the control membrane, the AA-modified and HEMA-modified membranes also showed a lower degree of flux decline and better flux recovery rate (>90%), suggesting that the membrane antifouling properties were improved and most of the fouling was reversible and could be removed via simple water cleaning process. We demonstrated in this work that the PECVD technique is a promising surface modification method that could be employed to rapidly improve membrane surface hydrophilicity (15 s) for the enhanced protein purification process without using any organic solvent during the plasma modification process.

This study focuses on the development of flat sheet thin film nanocomposite (TFN) pressure retarded osmosis (PRO) membranes for the enhancement of osmotic power generation by the incorporation of laboratory-synthesised graphene oxide (GO) into the polysulfone (PSf) polymer matrix. A series of membranes containing different weight percent of GO (0, 0.1, 0.25, 0.5 and 1.0 wt%) were fabricated via a phase inversion method with polyethylene glycol (PEG) as the pore forming agent. The results show that the TFN-0.25GO membrane has excellent water flux, salt reverse flux, high porosity and an enhanced microvoids morphology compared to the control membrane. The highest power density was achieved when TFN-0.25GO was used is 8.36 Wm−2 at pressure >15 bar. It was found that the incorporation of GO into the polymer matrix has significantly improved the intrinsic and mechanical properties of the membrane.

Simulation via Computational Fluid Dynamics (CFD) offers a convenient way for visualising hydrodynamics and mass transport in spacer-filled membrane channels, facilitating further developments in spiral wound membrane (SWM) modules for desalination processes. This paper provides a review on the use of CFD modelling for the development of novel spacers used in the SWM modules for three types of osmotic membrane processes: reverse osmosis (RO), forward osmosis (FO) and pressure retarded osmosis (PRO). Currently, the modelling of mass transfer and fouling for complex spacer geometries is still limited. Compared with RO, CFD modelling for PRO is very rare owing to the relative infancy of this osmotically driven membrane process. Despite the rising popularity of multi-scale modelling of osmotic membrane processes, CFD can only be used for predicting process performance in the absence of fouling. This paper also reviews the most common metrics used for evaluating membrane module performance at the small and large scales.

Membrane distillation (MD) is one of the emerging thermal driven membrane separation processes in wastewater treatment attributed to its lower energy requirement and able to couple with waste heat relative to pressure driven process. In this study, polyimide was used as the polymeric materials in hollow fiber membrane fabrication whereas 1-methyl-2-pyrrolidone (NMP) was use as solvent for synthesize industrial wastewater in nickel removal. The properties of the fabricated membrane were found to possesses the optimum characteristic in terms of LEP, porosity, inner diameter and morphology as reported in literature forthe application of DCMD. The permeate flux performance in the range of 67 to 79 kg/m2h with the rejectionrate of more than 98.80 % suggested that the PI membrane possesses the potential to be applied in the industrial wastewater treatment in nickel removal.