A Mini-Review of Enhancing Ultraﬁltration Membranes (UF) for Wastewater Treatment: Performance and Stability

: The scarcity of freshwater resources in many regions of the world has contributed to the emergence of various technologies for treating and recovering wastewater for reuse in industry, agriculture, and households. Deep wastewater treatment from oils and petroleum products is one of the difﬁcult tasks that must be solved. Among the known technologies, UF membranes have found wide industrial application with high efﬁciency in removing various pollutants from wastewater. It is shown that the search for and development of highly efﬁcient, durable, and resistant to oil pollution UF membranes for the treatment of oily wastewater is an urgent research task. The key parameters to improve the performance of UF membranes are by enhancing wettability (hydrophilicity) and the antifouling behavior of membranes. In this review, we highlight the using of ultraﬁltration (UF) membranes primarily to treat oily wastewater. Various methods of polymer alterations of the UF membrane were studied to improve hydrophilicity, the ability of antifouling the membrane, and oil rejection, including polymer blending, membrane surface modiﬁcation, and the mixed membrane matrix. The inﬂuence of the type and composition of the hydrophilic additives of nanoparticles (e.g., Multiwall carbon nanotubes (MWCNT), graphene oxide (GO), zinc oxide (ZnO), and titanium dioxide (TiO 2 ), etc.) was investigated. The review further provides an insight into the removal efﬁciency percent. validation, T.M.S., Q.F.A., A.F. and N.A.T.; formal analysis, E.S.A.; investigation, E.S.A., and I.K.S.; data curation, E.S.A. and Q.F.A.; writing—original draft preparation, E.S.A. and Q.F.A.; writing—review and editing, T.M.S., Q.F.A., A.F. and N.A.T.; visualization, E.S.A. and Q.F.A.; supervision, T.M.S., N.A.T., and Q.F.A. All authors


Introduction
The sustainable utilization of water resources is the mainstay for the sustainable development of modern society and the economy. As a result of the rapid development of the economy and society, the pressure on the shortage of water resources has increased due to industrial and human activities which consequently discharge most of their pollutants into the environment as sewage, waste, accidental discharges, etc. [1,2].
Various technologies have appeared to clean and restore polluted water for industrial, agricultural, and human consumption, such as screening, pre-sedimentation, coagulationflocculation, advanced oxidation processes (AOPs), and the filter membrane [3], as well as numerous techniques for the wastewater purification, containing conventional physical, chemical, biological, and membrane-based methods [4,5]. Advanced oxidation processes (AOPs) are an excellent technique for treating the contaminated wastewaters containing

Polymeric Membranes
Every polymeric material has specified properties, making them suitable for the preparation of different membranes for the application of various separation processes. In the last decade, researchers have focused their studies on using the polymeric membranes for a wide range of applications due to better pore-forming control, easy-forming properties, and inexpensive implementation to that of ceramic-based membranes as well as outstanding mechanical properties, good chemical resistance, and low energy requirements [7].
Polymeric membranes have disadvantages, such as disability to separate volatile compounds and the fouling phenomenon at the surface of the membrane that leads to reducing the permeation flux, especially for oily wastewater treatment [10]. In this regard, several approaches were conducted to improve hydrophilicity and antifouling membrane ability, long lifetimes, and oil rejection [31] by developed methods of polymer alterations which include (i) polymer-blending, (ii) membrane surface modification, and (iii) the mixed membrane matrix. Table 1 summarizes approaches for the polymeric membrane for oily wastewater treatment.

Polymer Blending
In the polymer-blending, several types of polymers are mixed together to produce miscible or immiscible dope solution. The blending approach was extensively utilized in polymeric membrane preparation owing to its ability to modify the properties of the membrane, and its versatility to integrate desired properties on the membrane [2]. The aim of the polymer-blending was used to enhance the final structural morphology, wettability, fouling resistance, and functionality of the membrane in order to improve water flux, antifouling properties, and the oil rejection rate [31].
In Masuelli et al.'s work, improvement of the PVDF/sulfonated polycarbonate (SPC) membrane was investigated. The blend-charged membranes were prepared by treating the polycarbonate with acetyl sulphate, then blended SPC with 5 wt% PVP and 15 wt% PVDF polymer at 50 • C. By using a film extensor, the finished mixture was cast onto the non-woven support. Membranes are then preserved in a water bath until they are needed. The different SPC/PVDF ratios and its oil rejection coefficient (R) for blend membranes are shown in Table 2. Whereas the resulting membrane had a high oil rejection efficiency (>96.63%), the fouling resistance reduced in membranes when it was prepared by using 2 to 4 wt.% SPC. The SEM microphotographs of the membranes are shown in Figure 1, which shows that SPC has a minor effect on the structure of the membrane: in the presence of SPC, the porous substructure densifies [32].
In the other study, Zhu et al. prepared superhydrophilic zwitterionic PVDF/PSH [poly (3-(N-2-methacryloxyethyl-N, N-dimethyl) ammonato propane sultone)-co-2-hydroxyethylmethacrylate] by using non-solvent induced phase inversion (NIPS). A copolymer poly (dimethylaminoethyl methacrylate-co-2-hydroxyethyl methacrylate) (PDH) was created as a zwitterionic polymer precursor and employed as an additive in membrane preparation to make this zwitterionic PVDF membrane. PVDF and PDH were blended in n-methyl-2-pyrrolidone (NMP). The former and the latter have fluxes of 3850 and 6350 L/m 2 h, respectively. The blending membrane PVDF/PSH showed super hydrophilicity and superoleophobicity due to the presence of zwitterionic sulfonate groups on the membrane layer. Furthermore, the membrane has the flux recovery of 98% [33].   Besides, polyamide imide-sulfonated poly (ether keton) (PAI-SPEEK) blend hollow fibers for oily wastewater treatment were prepared and investigated extensively by Johari et.al. [34]. Due to an excellent processability for membrane fabrication resulting from the flexible amide groups which can be an attractive amorphous thermoplastic polymer, the porosity was about 79%, the outer surface water contact angle 58 • , and the mean pore size 12 nm and 81 nm for the membrane prepared by a PAI/SPEEK ratio of 85/15, respectively. The morphological structure and performance of the membrane was tested by FESEM analysis (Figure 2) and UF experiments ( Figure 3). From Figure 2, it is found that the membranes have about 0.4 mm and 0.65 mm for an inner diameter and an outside diameter, respectively. In general, the final membrane morphology is concerning with (thermodynamic and kinetic) effects of the polymer solution. Images show that the larger finger-like cavities were expanded from the outer surface into the membrane matrix by increasing the PAI/SPEEK ratio. Their results showed that the membrane was workable for the UF of oily wastewater treatment and the oil rejection over 95% [34].
The morphological structure and performance of the membrane was tested by FESEM analysis (Figure 2) and UF experiments ( Figure 3). From Figure 2, it is found that the membranes have about 0.4 mm and 0.65 mm for an inner diameter and an outside diameter, respectively. In general, the final membrane morphology is concerning with (thermodynamic and kinetic) effects of the polymer solution. Images show that the larger finger-like cavities were expanded from the outer surface into the membrane matrix by increasing the PAI/SPEEK ratio. Their results showed that the membrane was workable for the UF of oily wastewater treatment and the oil rejection over 95% [34].
Moreover, similar findings were documented by Chakrabarty et al. who observed a major effect on permeate flux and the removal of oil droplet (>90%) by blend membranes composed of PSf, polyethylene glycol (PEG), and polyvinylpyrrolidone (PVP) of various molecular weights. It is noticed that the morphological membranes' properties were clearly changed by the addition of various molecular weights of PVP and PEG [22].

Surface Modified-Membranes
Recently, great interest has been focused on modifying the membranes' surface to enhance membrane performance. A significant criterion for surface modification is im- Moreover, similar findings were documented by Chakrabarty et al. who observed a major effect on permeate flux and the removal of oil droplet (>90%) by blend membranes composed of PSf, polyethylene glycol (PEG), and polyvinylpyrrolidone (PVP) of various molecular weights. It is noticed that the morphological membranes' properties were clearly changed by the addition of various molecular weights of PVP and PEG [22].

Surface Modified-Membranes
Recently, great interest has been focused on modifying the membranes' surface to enhance membrane performance. A significant criterion for surface modification is improved antifouling and performance which has become a main factor in membrane engineering. Surface modification of the membrane can be produced by either physical (plasma irradiation, Ion beam irradiation, and vapor phase deposition) or chemical techniques (coating, grafting, and acid base treatment) [19]. Zhang et al. used the alkali-induced phase inversion process to prepare PAN UF membranes. The NaOH is added to the coagulation bath as an additive to induce the wetting property of the PAN membrane through the alkaline-induced phase inversion process, which results in the creation of a rough structure on the membrane surface. The porosity of the PAN membranes prepared in pure water was 64.2%, while the porosity of the PAN membranes prepared in the NaOH coagulating bath was substantially higher at (71.7, 75.1, 79.6)%, corresponding to NaOH concentrations of (2, 5, 10)%, respectively. The results showed a superior recyclability and antifouling due to its ultra-low oil adherence property and permeation flux of 2270 L/m 2 h with an oil removal efficiency of 85% [28].
Moreover  Table 3. The results showed that the oil rejection is 91.5%. The best performance was achieved in (M-3) by the embedding of 1 wt.% of carboxylated TiO 2 nanoparticles in PVA-coated PVDF membranes as shown in Figure 4, which explains schematically the effect of the carboxylated TiO 2 nanoparticles on the structure and performance of the membrane. After carboxylation, TiO 2 nanoparticles are more compatible with PVA, so an increase in the number of cross linkages between the PVA hydroxyl moieties and acid groups on the surface of TiO 2 is expected. In addition, it clarifies the well-dispersed TiO 2 nanoparticles within the PVA (M-3) vs. agglomeration of TiO 2 bonded to PVA (M-4), and a lower rejection of solutes was observed [35]. Wandera et al. suggested grafting poly (N-isopropylacrylamide) (PNIPAAm)-block poly (oligo ethylene glycol methacrylate) (PPEGMA) nanolayers from the surface of the membrane to modify the surface of low molecular weight cutoff regenerated cellulose UF membranes, with the aim to prepare antifouling surfaces for produced water treatment. The modification of the membrane enhanced the TOC removal up to 97% with the reduction in the fouling rate [36]. The same surface modification technique (graft modification) was used by Masuelli et al. for treating oily wastewater by changing the charge of the PVDF membranes. Glycidyl methacrylate (GMA) and ethylene glycol dimethacrylate (EDMA) were utilized as monomers in the grafting polymerization step followed by sulfonation using sodium sulfite. The charged PVDF membranes showed about 98% of oil emulsion rejection [37]. sion from ref. [35]. © 2015 Elsevier B.V. Wandera et al. suggested grafting poly (N-isopropylacrylamide) (PNIPAAm)-blo poly (oligo ethylene glycol methacrylate) (PPEGMA) nanolayers from the surface of t membrane to modify the surface of low molecular weight cutoff regenerated cellulose U membranes, with the aim to prepare antifouling surfaces for produced water treatme The modification of the membrane enhanced the TOC removal up to 97% with the redu tion in the fouling rate [36]. The same surface modification technique (graft modificatio was used by Masuelli et al. for treating oily wastewater by changing the charge of t PVDF membranes. Glycidyl methacrylate (GMA) and ethylene glycol dimethacryla (EDMA) were utilized as monomers in the grafting polymerization step followed by s fonation using sodium sulfite. The charged PVDF membranes showed about 98% of emulsion rejection [37].

Mixed Matrix Membranes (MMM)
A typical mixed matrix membrane MMM is fabricated by mixing an inorganic par cle-such as silicon dioxide (SiO2), carbon nanotubes (CNTs), ZnO, and TiO2-within matrix of the polymer. The MMM takes some of the characteristics of inorganic particl especially their superior performance of separation. The main purpose of this mixing w

Mixed Matrix Membranes (MMM)
A typical mixed matrix membrane MMM is fabricated by mixing an inorganic particlesuch as silicon dioxide (SiO 2 ), carbon nanotubes (CNTs), ZnO, and TiO 2 -within a matrix of the polymer. The MMM takes some of the characteristics of inorganic particles, especially their superior performance of separation. The main purpose of this mixing was to incorporate the beneficial properties of the two types of materials, thus enhancing the overall effectiveness. In the current decade, research using MMM has attracted more interest than polymer blending, as it has a greater ability to eliminate particular contaminants and the low fouling phenomenon [41].
The antifouling properties and permeability performance of the membrane were enhanced when adding SiO 2 nanoparticles into the blended composition, found by Ahmad nants and the low fouling phenomenon [41].
The antifouling properties and permeability performance of the membrane were enhanced when adding SiO2 nanoparticles into the blended composition, found by Ahmad et al. through fabricating the PSf MMM. For the modified membrane, the permeate flux (PSf-5) (17.32 L/m 2 h) showed 16 times an increment in membrane permeability compared to the unmodified membrane (PSf-0) (1.08 L/m 2 h) ( Figure 5) [23]. Besides, TiO2 was also used to increase the membrane hydrophilicity in MMMs PVDF UF membranes were fabricated by Lithium Chloride monohydrate (LiCl·H2O) and TiO2 nanoparticles by Yuliwati and Ismail for treating oily wastewater using MMM. At (1.95 wt.%) TiO2, the membrane presented a maximum flux (82.5 L/m 2 h) and an oil removal rejection of (98.83%), respectively [38]. Similar work was also studied by Ong et al where they discovered that at (2 wt.%) TiO2, the PVDF-TiO2 membrane had the highest flux [39].
Moreover, Ong et al. studied hollow fiber MMM at various concentrations of TiO2 in the PVDF and found that with the addition of PVP, the membrane showed that the added (2 wt.%) TiO2 concentration in the PVDF membrane played an important role in improving membrane structure by enhancing membrane hydrophilicity, pore size, and surface roughness at a (2 wt.%) TiO2 concentration . The presence of hydrophilic PVP with TiO2 nanoparticles had substantially improved membrane porosity. The porosity was found to be (84.10-88.60%), the water contact angle was (68.40-75.70)°, and the pore size was (94.30-104.40) nm. the PVDF-TiO2 membrane had the water flux 70.48 L/m 2 h and oil rejection 99.7% [40]. In addition, Yi et al. used TiO2/Al2O3 with PVDF MMM for oil/water emulsion separation. The results showed a better antifouling pattern when using modified PVDF membranes compared to the pristine PVDF membrane under the same conditions [41]. Besides, TiO 2 was also used to increase the membrane hydrophilicity in MMMs. PVDF UF membranes were fabricated by Lithium Chloride monohydrate (LiCl·H 2 O) and TiO 2 nanoparticles by Yuliwati and Ismail for treating oily wastewater using MMM. At (1.95 wt.%) TiO 2 , the membrane presented a maximum flux (82.5 L/m 2 h) and an oil removal rejection of (98.83%), respectively [38]. Similar work was also studied by Ong et al. where they discovered that at (2 wt.%) TiO 2 , the PVDF-TiO 2 membrane had the highest flux [39].
Moreover, Ong et al. studied hollow fiber MMM at various concentrations of TiO 2 in the PVDF and found that with the addition of PVP, the membrane showed that the added (2 wt.%) TiO 2 concentration in the PVDF membrane played an important role in improving membrane structure by enhancing membrane hydrophilicity, pore size, and surface roughness at a (2 wt.%) TiO 2 concentration. The presence of hydrophilic PVP with TiO 2 nanoparticles had substantially improved membrane porosity. The porosity was found to be (84.10-88.60%), the water contact angle was (68.40-75.70) • , and the pore size was (94.30-104.40) nm. the PVDF-TiO 2 membrane had the water flux 70.48 L/m 2 h and oil rejection 99.7% [40]. In addition, Yi et al. used TiO 2 /Al 2 O 3 with PVDF MMM for oil/water emulsion separation. The results showed a better antifouling pattern when using modified PVDF membranes compared to the pristine PVDF membrane under the same conditions [41].

Membranes Structure and Performance
Membrane performance depends on its structure that is controlled through membrane synthesis methods, polymer (type and composition), and additives (type and composition). To gain the desirable performance of the membrane, many researchers investigated the effect of (i) membrane synthesis techniques, (ii) polymer selection and alterations methods, (iii) additives type and their concentration, etc. on the morphology of the membrane and thus on membrane performance.

Phase Inversion Technique
In the phase inversion technique or method, a de-mixing process in which at first a polymer solution with a homogeneous form is converted from a liquid phase to a solid phase in a controlled mode. This technique is commonly utilized to prepare polymeric membranes with a porous structure. In the phase inversion method, any polymer-if it is soluble in a solvent or mixture of solvents-can be utilized to fabricate a membrane. The performance and morphology of the membrane can be improved by controlling the polymer-solvent interaction through a choice of a suitable solvent [48,49].
The phase inversion technique is commonly used to prepare asymmetric polymeric membranes. Various methods are utilized to precipitate polymer solutions in the phase inversion technique, such as immersion precipitation or non-solvent induced phase inversion (NIPS), evaporation induced phase inversion (EIPS), vapor induced phase inversion (VIPS), and thermally induced phase inversion (TIPS). Due to easier preparation of NIPS, it is considered to be the most widely used technique among phase inversion techniques for preparation of polymeric membranes for the desired morphology [8,11].
Alkindy et al. fabricated a PES-based GO-SiO 2 membrane for oily wastewater treatment by the phase inversion technique, as shown in Figure 6. PES/GO-SiO 2 membrane was prepared using a loading concentration of (1.0 wt.%) of the nanoparticle to the polymer. The nanoparticle was dispersed in DMAc and ultrasonicated in a water bath for 30 min. PVP (4 wt.%) was dissolved in the solution followed by the addition of PES (16 wt.%) and stirred for 24 h at 60 • C. The dope solution was set aside for 24 h to remove trapped air bubbles (i.e., membrane degassing). The solution was subsequently cast on a polyester membrane support on clean glass at a thickness of 200 µm. The glass plate was immersed horizontally into deionized (DI) water at a temperature of 25 • C for 24 h. Finally, the membranes were washed with DI water and stored for use. The membrane showed the highest water flux (2561 LMH) and a 38% increase in oil removal efficiency in comparison to a PES membrane [20].
min. PVP (4 wt.%) was dissolved in the solution followed by the addition of PES (16 wt.%) and stirred for 24 h at 60 °C. The dope solution was set aside for 24 h to remove trapped air bubbles (i.e., membrane degassing). The solution was subsequently cast on a polyester membrane support on clean glass at a thickness of 200 μm. The glass plate was immersed horizontally into deionized (DI) water at a temperature of 25 °C for 24 h. Finally, the membranes were washed with DI water and stored for use. The membrane showed the highest water flux (2561 LMH) and a 38% increase in oil removal efficiency in comparison to a PES membrane [20]. Zhu et al. prepared novel membranes by introducing nanohybrid particles (GO/SiO2) and polyvinylpyrrolidone (PVP) into PVDF polymer solution through the phase inversion technique. GO and SiO2 nanoparticles were sonicated for 1 h after being applied to (0.3 wt.%) DMAC solvent. Polyvinyl pyrrolidone (PVP) powder and PVDF powder were added successively and stirred until the PVDF material had fully dissolved. The homogeneous polymer solution was permitted to fix at 60 °C for 12 h for deaeration. After extracting the bubbles, the polymer solution was cast onto a glass board. After that, the glass board was immersed horizontally in pure water at 20 °C for 24 h to extract the solvent by the coagulation bath. At the end, the membrane was washed frequently with DI water, and kept in it at 4 °C. Figure 7 shows the SEM cross sections and the AFM image of the nanohybrid membrane. The SEM cross section shows that the membrane has a composite porous structure with a skin layer and a characteristic asymmetric finger-like porous sublayer, and the AFM image shows many serrated and conical protrusions seemingly on the surface of the PVDF/GO@ SiO2/PVP membrane, due to the difference in the roughness of the membrane which contributed to the nucleation and growth of the polymer produced by the addition of nanofillers [47]. Zhu et al. prepared novel membranes by introducing nanohybrid particles (GO/SiO 2 ) and polyvinylpyrrolidone (PVP) into PVDF polymer solution through the phase inversion technique. GO and SiO 2 nanoparticles were sonicated for 1 h after being applied to (0.3 wt.%) DMAC solvent. Polyvinyl pyrrolidone (PVP) powder and PVDF powder were added successively and stirred until the PVDF material had fully dissolved. The homogeneous polymer solution was permitted to fix at 60 • C for 12 h for deaeration. After extracting the bubbles, the polymer solution was cast onto a glass board. After that, the glass board was immersed horizontally in pure water at 20 • C for 24 h to extract the solvent by the coagulation bath. At the end, the membrane was washed frequently with DI water, and kept in it at 4 • C. Figure 7 shows the SEM cross sections and the AFM image of the nanohybrid membrane. The SEM cross section shows that the membrane has a composite porous structure with a skin layer and a characteristic asymmetric finger-like porous sublayer, and the AFM image shows many serrated and conical protrusions seemingly on the surface of the PVDF/GO@ SiO 2 /PVP membrane, due to the difference in the roughness of the membrane which contributed to the nucleation and growth of the polymer produced by the addition of nanofillers [47].  Table 5 summarizes the interfacial polymerization conditions. Firstly, the PVDF fiber was kept in an aqueous solution containing acetone of varying concentrations and 2 wt.% monomer m-phenylenediamine (MPD) for 5 min. The wet PVDF was contacted to an organic phase consisting of 0.5 wt.% TMC/toluene solution for 2 min, and then a PA layer formed immediately. Finally, the membrane was dried by air for 10 min to obtain extra polymerization; the ATR- Then, the PMMA-MWCNTs and trimesoyl chloride (TMC) solution in toluene were poured at the PIP-soaked substrate. At ambient pressure, the PA-TFN membrane was put in an oven at 80 • C in air. Then, the TFN membranes were kept in DI water and stored at 20 • C before use, resulting in the pure water flux (∼1.94 × 10 −3 cm 3 /cm 2 ·s) through PMMA-MWCNTs (0.67 wt.%)/PA (PIP/TMC) membrane [42].
Marquez et al. prepared thin-film composite PA membranes by cosolvent-assisted interfacial polymerization on the external surface of PVDF fiber. Table 5 summarizes the interfacial polymerization conditions. Firstly, the PVDF fiber was kept in an aqueous solution containing acetone of varying concentrations and 2 wt.% monomer m-phenylenediamine (MPD) for 5 min. The wet PVDF was contacted to an organic phase consisting of 0.5 wt.% TMC/toluene solution for 2 min, and then a PA layer formed immediately. Finally, the membrane was dried by air for 10 min to obtain extra polymerization; the ATR-FTIR spectra of PVDF and thin film composite PA/PVDF fiber are shown in Figure 8. The water concentration and the permeation flux were 99.88 wt.% and 1654.98 L/m 2 h, respectively [43].

Spray-Assisted Layer-by-Layer Technique
Ma et al. established a highly efficient spray-and spin-assisted layer-by-layer (SSLbL) method for functionalizing thin film composite TFC-PA membranes with controllable copper nanoparticles CuNPs for biofouling power. A membrane coupon was adhered to a polycarbonate plate and rotated at 2000 rpm while being sprayed coated (2.1 bar). The membrane was swilled with DI water between each layer deposition and dried in the air for 10 s (with only spinning). This process completed one step of LbL deposition, resulting in a single polyethyleneimine-CuNPs/poly (acrylic) acid (PEI-CuNPs/PAA) bilayer. Multi-layer coating showed a minor impact on the water permeation flux (13.3% reduction). CuNPs could enhance the anti-biofouling property of a PA membrane and efficiently inhibit the permeate flux reduction caused by bacterial deposition on the membrane surface [44].
Liu et al. used a spray-assisted layer-by-layer technique to fabricate the PES/F-MWCNTs membrane. The F-MWCNTs were added to ethanol aqueous solution and ultrasonicated; after that, it was mixed with MWCNTs solution to form a homogeneous poly (sodium 4-styrenesulfonate) PSS solution with MWCNTs content with the aid of another ultrasonication. The poly (diallyl-dimethylammonium chloride) (PDDA) polymer was

Spray-Assisted Layer-by-Layer Technique
Ma et al. established a highly efficient spray-and spin-assisted layer-by-layer (SSLbL) method for functionalizing thin film composite TFC-PA membranes with controllable copper nanoparticles CuNPs for biofouling power. A membrane coupon was adhered to a polycarbonate plate and rotated at 2000 rpm while being sprayed coated (2.1 bar). The membrane was swilled with DI water between each layer deposition and dried in the air for 10 s (with only spinning). This process completed one step of LbL deposition, resulting in a single polyethyleneimine-CuNPs/poly (acrylic) acid (PEI-CuNPs/PAA) bilayer. Multilayer coating showed a minor impact on the water permeation flux (13.3% reduction). CuNPs could enhance the anti-biofouling property of a PA membrane and efficiently inhibit the permeate flux reduction caused by bacterial deposition on the membrane surface [44].
Liu et al. used a spray-assisted layer-by-layer technique to fabricate the PES/F-MWCNTs membrane. The F-MWCNTs were added to ethanol aqueous solution and ultrasonicated; after that, it was mixed with MWCNTs solution to form a homogeneous poly (sodium 4-styrenesulfonate) PSS solution with MWCNTs content with the aid of another ultrasonication. The poly (diallyl-dimethylammonium chloride) (PDDA) polymer was spiked into DI water to prepare PDDA aqueous solution. The PES substrates were soaked in DI water at 25 • C for 24 h for removing the wetting agent of the membrane. The pure water flux of the bare PES membrane was reduced with more bilayer deposition of polyelectrolyte/MWCNTs [45].

Polymer Grafting Technique
Wandera et al. used grafting PNIPAAm-b-PPEGMA nanolayers by surface-initiated atom transfer radical polymerization (ATRP) to modify the surface of low molecular weight cutoff regenerated cellulose UF membranes, with the aim to fabricate antifouling surfaces for produced water treatment. Figure 9 shows how to use surface-initiated ATRP to modify a regenerated cellulose UF membrane with PNIPAAm-b-PPEGMA. After contacting ATRP initiator molecules with the membrane, surface-initiated ATRP was used to graft PNIPAAm chains from the initiator groups. Then, by re-starting PNIPAAm chains, PPEGMA (as the second polymer block) was grafted. The rejection was up to 97%, and the fouling rate decreased [36].

Polymer Grafting Technique
Wandera et al. used grafting PNIPAAm-b-PPEGMA nanolayers by surface-initiated atom transfer radical polymerization (ATRP) to modify the surface of low molecular weight cutoff regenerated cellulose UF membranes, with the aim to fabricate antifouling surfaces for produced water treatment. Figure 9 shows how to use surface-initiated ATRP to modify a regenerated cellulose UF membrane with PNIPAAm-b-PPEGMA. After contacting ATRP initiator molecules with the membrane, surface-initiated ATRP was used to graft PNIPAAm chains from the initiator groups. Then, by re-starting PNIPAAm chains, PPEGMA (as the second polymer block) was grafted. The rejection was up to 97%, and the fouling rate decreased [36].

Polymer Selection and Alterations Methods
Membrane hydrophilicity, as well as chemical, mechanical, and thermal stability of the membrane, are influenced by the polymer selection. During membrane synthesis, it plays a vital role because solvent selection depends on the polymer solubility in the solvent [8].
Various approaches, such as physical blending, chemical grafting, and surface modifications, were used in several studies to enhance membrane performance [50]. The physical blending polymer is one of these methods that has gotten a lot of attention because of the materials' comfortable operations, mild conditions, and good performances [38,51]. The effect of the polymer alterations methods on the membrane performance is described in Sections 2 in detail.

Type of the Nanoparticle (NPs) Additives
Development of antifouling membranes is an intensive research area in membrane engineering. Using nanoparticles in fabricating membranes allows the ability to produce the desired structure of membranes which enhances the property of the membrane materials, and a high degree of control of the membrane fouling and permeability as well as the permeability quality [52]. Modifying the hydrophilic group on the membrane surface and creating micro-nanostructures on the surface of the membrane to increase roughness improved the membrane's hydrophilicity [53].
Nanoparticles (NPs) are classified into many groups based on their size, shape, and chemical and physical properties. Some of them are polymeric nanoparticles, carbonbased NPs, semiconductor NPs, ceramic NPs, lipid-based NPs, and metal NPs [54]. The nanoparticles that have been embedded in the matrix of the membrane are MWCNTs, halloysite nanotubes (HNTs), TiO2, MgO, SiO2, GO, ZnO, etc. [4]. Table 6 summarized the

Polymer Selection and Alterations Methods
Membrane hydrophilicity, as well as chemical, mechanical, and thermal stability of the membrane, are influenced by the polymer selection. During membrane synthesis, it plays a vital role because solvent selection depends on the polymer solubility in the solvent [8].
Various approaches, such as physical blending, chemical grafting, and surface modifications, were used in several studies to enhance membrane performance [50]. The physical blending polymer is one of these methods that has gotten a lot of attention because of the materials' comfortable operations, mild conditions, and good performances [38,51]. The effect of the polymer alterations methods on the membrane performance is described in Section 2 in detail.

Type of the Nanoparticle (NPs) Additives
Development of antifouling membranes is an intensive research area in membrane engineering. Using nanoparticles in fabricating membranes allows the ability to produce the desired structure of membranes which enhances the property of the membrane materials, and a high degree of control of the membrane fouling and permeability as well as the permeability quality [52]. Modifying the hydrophilic group on the membrane surface and creating micro-nanostructures on the surface of the membrane to increase roughness improved the membrane's hydrophilicity [53].
Nanoparticles (NPs) are classified into many groups based on their size, shape, and chemical and physical properties. Some of them are polymeric nanoparticles, carbonbased NPs, semiconductor NPs, ceramic NPs, lipid-based NPs, and metal NPs [54]. The nanoparticles that have been embedded in the matrix of the membrane are MWCNTs, halloysite nanotubes (HNTs), TiO 2 , MgO, SiO 2 , GO, ZnO, etc. [4]. Table 6 summarized the type of NPs and effect on the membrane performance.

Carbon-Based Nanoparticles
CNTs are one of the most common types of carbon-based NPs. CNTs have an elongated, tubular structure and can be single named as single-walled (SWNTs), double named as double-walled (DWNTs), or many walls named as multi-walled carbon nanotubes (MWCNTs) [54]. MWCNTs were one of the strong additives with remarkable properties such as high thermal conductivity, individual mechanical property, and high specific surface area. The addition of functionalized MWCNTs allows high permeation flux due to reducing the formation boundary layers at the membrane surface and raising the membrane surface roughness [9].
As an example of the research works found in the literature that used CNTs as embedded material, Saadati and Pakizeh prepared a new PSf/pebax/F-MWCNTs nanocomposite membrane for oil/water emulsion. For enhancing the membrane characteristics, (0.5, 1, and 2) wt.% of F-MWCNT was applied to pebax solution, achieving the higher permeate flux at (0.5 wt.%) F-MWCNTs and the best oil rejection at (2 wt.%) F-MWCNTs [24]. Zarghami et al.  Figure 11. The developed membranes present high oil rejection (>99%) and flux (~1086%) compared to the undeveloped PES membrane. Moreover, evaluation of the modified membrane in cross-flow filtration produced its antifouling properties through the long-term application (16 r) [21]. Moreover, MWCNTs were used by Jalal et al. to fabricate (PVC/MWCNT-g-GO) membranes for treating refinery wastewater. The permeation flux of (0.119 wt.%) MWCNT-g-GO was 254 L/m 2 h, and the COD rejection increased dramatically from (60%) neat PVC to (88.9%) for both membranes made from PVC plus (0.119 or 0.219) wt.% of MWCNT-g-GO [36]. In addition, the PVDF/MWCNTs nanocomposite membrane system was developed by Moslehyani et al. The experiment was conducted by comparing neat PVDF, original PVDF/MWCNTs, and oxidized PVDF/MWCNTs ( Figure 12) with water fluxes of (50, 520, and 700) L/m 2 h, respectively, in one hour [55].

Semiconductor Nanoparticles
Semiconductor materials have properties that are similar to both metals and nonmetals, so a wide range of semiconductor NPs are extremely effective in water applications. Some examples of semiconductor nanoparticles are ZnO, ZnS, GaN, GaP, CdS, and CdSe [54].
One of the popular low-cost semiconductor NPs is ZnO; this NPs was used by Alsalhy et al. to prepare polyphenylsulfone PPSU/ZnO-NPs membranes, and they found that the hydrophilicity, mean roughness, and mean pore size were improved by increasing the ZnO-NPs concentration. The permeate flux was significantly enhanced (i.e., 76-107 L/m 2 h) with the addition of (0.025 wt.%) ZnO-NPs [56].

Ceramic Nanoparticles
Ceramic nanoparticles consist mostly of oxides, carbides, phosphates, and metal carbonates and metalloids such as calcium, titanium, silicon, etc. Because of their chemical inertness and high heat resistance, it is possible to use them in a wide range of applications. Some examples of ceramic NPs are silica (SiO 2 ), titanium oxide (TiO 2 ), alumina (Al 2 O 3 ), hydroxyapatite (HA), and zirconia (ZrO 2 ) [54]. Several researchers utilized the ceramic NPs as an additive in polymer solution; for example, Li et al. used SiO 2 -GO to prepare a PVDF/SiO 2 -GO nanohybrid; the TEM images of GO and SiO 2 -GO nanosheets are shown in Figure 13. The results showed that when the (0.9 wt.%) concentration of SiO 2 -GO was added in the PVDF solution, the PVDF/SiO 2 -GO membrane (M-4) produced the lowest permeation flux (182.6 L/m 2 h) and a higher removal (91.7%). However, the over-high addition of SiO 2 /GO (1.2 wt.%) leads to the superior permeation flux (679.1 L/m 2 h) [57]. The SiO 2 /GO nanohybrid particles were also used by Zhu et al. to prepare the PVDF/GO@SiO 2 /PVP membranes. The synthesis process, and the TEM and FESM images of nanoparticles GO@SiO 2 , are shown in Figures 14 and 15, respectively. Figure 14 shows the synthesis process of nanoparticles GO-SiO 2 , and the C-O-Si structure was formed on the GO surface, which made it so that the nano-silca particles were firmly attached to the surface of GO, and Figure 15 shows SiO 2 particles as "black balls" and "white balls" which are dispersed homogeneously between the GO sheets. The PVDF/GO@SiO 2 /PVP membrane had much lower adhesion forces than PVDF/PVP membranes, implying that the PVDF/GO@SiO 2 /PVP membrane has superior performance and antifouling capabilities among nanohybrid membranes. Due to the effects of GO/SiO 2 and PVP, the membrane had higher rejection, higher flux, and a great ability of antifouling [47].
The TiO 2 had received most attention due to its ease of preparation, stability under harsh conditions, and commercial availability. It is an ideal material for preparing a composite membrane for oil/water separation, as it can achieve excellent oleophobicity and smooth water filtration that reduce membrane fouling. Wu et al. fabricated the membrane by assembling TiO 2 nanotubes and GO nanosheets for oil/water separation, which improved the hydrophilicity, permeability, and anti-oil-fouling ability of the membranes [53]. Reprinted with permission from ref. [57]. © 2016 Elsevier B.V. Reprinted with permission from ref. [57]. © 2016 Elsevier B.V.

UF Membranes Applications in Oily Wastewater Treatment
Among all applications of UF membrane, it has been widely applied for wastewa treatment especially for oily wastewater applications. Table 7 shows the summary of t UF membrane applications in oily wastewater. For example, the PVDF-based UF me

UF Membranes Applications in Oily Wastewater Treatment
Among all applications of UF membrane, it has been widely applied for wastewater treatment especially for oily wastewater applications. Table 7 shows the summary of the UF membrane applications in oily wastewater. For example, the PVDF-based UF membrane was fabricated by Yuliwati et al., using LiCl.H 2 O and TiO 2 as embedded materials in PVDF solution for the application of refinery wastewater treatment. TiO 2 with (1.95%) and (0.98%) of LiCl.H 2 O in PVDF solution results in achieved water flux of (82.5 L/m 2 h) and (98.8%) oil rejection. The permeate flux reduced significantly when the TiO 2 is excess over (0.98%), due to poor dispersion of TiO 2 in the membrane matrix [58]. A similar study using the PVDF membrane was conducted by Liu et al. In their study, the polyaniline PANI-modified PVDF membrane was utilized for oily wastewater treatment, and they found the water flux up to 3000 L/m 2 h, high oil rejection, and high and steady flux of water permeation [59].
Moreover, the role of sulfonated polyphenyl sulfone (SPPSU) with the existence of the MgO nanoparticle for the oil/water emulsions treatment was investigated by Arumugham et al. [60]. The membrane made by using (25 wt.%) SPPSU/MgO leads to an enhanced flux recovery ratio (FRR) to (94.9%) due to the improvement of the hydrophilicity of the SPPSU/MgO membrane, which gives high oil rejection (≥99%) and a water flux of (234 L/m 2 h) [60].
In other studies carried out by Gohari et al. [61] and Kumar et al. [62], they used the PSf membrane for the treatment of an oil/water emulsion. Gohari et al. used hydrous manganese oxide (HAO) nanoparticles blended with the PSf membrane and enhanced the rejection (R) to (∼100%) and a water flux of (1194 L/m 2 h) by using a HAO:PSf weight ratio of (2:1) [61]. However, Kumar et al. found that the impact of 10−15 wt.% in the CS on the PSf results in enhanced R with a reduced permeate flux due to the reduction in the porosity of the membrane [62].
Ahmad et al. fabricated the PVC/DMAc/bentonite membrane to enhance the performance of the PVC-based UF membrane for the treatment of oily wastewater with an oil concentration 200 ppm. At 6.0 wt.% bentonite in the CS, an enhanced PVC membrane performance with water flux (186 L/m 2 h) was obtained due to the pore density, porosity, and hydrophilicity of the membrane [63].
In addition, PES MMM blended with hydrous manganese oxide (HMO) nanoparticles prepared by Gohari et al. for oily wastewater treatment (containing 1000 ppm oil) found a high water flux of (573.2 L/m 2 h), an oil rejection of (∼100%), and a FRR of (75.4%) [17].
The impact of varying concentrations of polyethylene glycol (PEG) on the morphology and performance of the PAN UF membrane was studied by Panda et al. [64]. At a PEG concentration of (0.08 g/g), the water flux was enhanced to (60 L/m 2 h), and the water flux reduced to (50 L/m 2 h) with a further increase in PEG concentration [64].

Conclusions
Considerable efforts are being undertaken in finding effective technologies for oily wastewater treatment. Membrane technology is one of the promising methods for treating oily wastewater. Among all types of membrane technology, ultrafiltration (UF) is considered to be a versatile separation process and purification process. It is commonly used to treat oily wastewater with <400 ppm oil content and <20 µm oil droplet size.
However, its widespread use requires improving the characteristics of polymer membranes in order to solve the problems of clogging. For the separation of oily wastewater, the low-cost super hydrophilic polymeric UF membrane with enhanced morphology and mechanical strength is in high demand. As a result, low-cost PES, PVC, PSf, and other polymers may be employed as a basis polymer.
Several methods of polymer alterations were used to improve hydrophilicity, antifouling membrane ability, and oil rejection, including polymer blending, membrane surface modification, and the mixed membrane matrix. Since fouling usually occurs on the surface of membrane, surface modification is one of the most reliable and simple methods to apply. The main purpose of membrane modification is to provide high permeate flux and hydrophilicity, improve surface morphology, and thus improve membrane performance.
Moreover, another approach has been tried to improve the performance of polymeric membranes with a beneficial effect by using additives such as inorganic nanoparticles, hydrophilic polymers, and amphiphilic and grafted copolymers. Popular inorganic particles that have been repeatedly used to fabricate membranes are SiO 2 , TiO 2 , Al 2 O 3 , MgO, GO, etc. Their use in membranes has significantly improved their antifouling properties with respect to oil products. This means that it is possible to prevent pollution of the environment with highly toxic oil products and to provide a source of clean water for recycling the water supply.

Conflicts of Interest:
The authors declare no conflict of interest.