Issam K. Salih

In this study, mesoporous silica nanoparticles (MSNs) with a hexagonal structure and large surface area were synthesized via a sol-gel method. The properties of the synthesized MCM-41 catalyst were characterized using BET, EDX, XRD, and FTIR analyses. The results showed that the MCM-41 had a high surface area of 966 m2/g and large pore volume of about 0.91 cm3/g. Sunflower oil was converted to biodiesel in a batch reactor at different temperatures (40, 50, 60 °C), methanol-to-oil molar ratios (6:1, 9:1, 12:1), catalyst loadings (0.7, 0.9, 1.25 wt%), and reaction times (up to 80 min) using the prepared catalyst under atmospheric pressure. The biodiesel yield was found to reduce when the reaction time exceeded 1 hour despite maintaining the catalyst. The maximum biodiesel yield of 45% was obtained under optimal conditions of a 9:1 methanol-to-oil ratio, 1.25 wt% catalyst loading, 60 °C temperature, and 60 min reaction time. GC-MS analysis characterized the biodiesel composition and properties. The synthesized biodiesel showed improved properties compared to conventional fuels, with linoleic acid methyl ester (C17H34O2, 25.93%) as the main component. The MCM-41 catalyst exhibited remarkable catalytic activity and could be recovered, regenerated, and reused, reducing reaction costs. This makes it a potential alternative to homogeneous catalysts that complicate product separation.

MCM-41, a mesoporous silica with a high surface area and hexagonal structure, was synthesized, and commercial nano-silicon dioxide (SiO₂) was used as a solid adsorbed in post-combustion CO₂ capture. The CO₂ adsorption experiments were conducted in a fixed-bed adsorption system using 5–15 vol.% CO₂/N₂ at a flow rate of 100 mL/min at varying temperatures (20–80 °C) and atmospheric pressure. Analyses (X-ray diffraction, nitrogen adsorption-desorption isotherms, Fourier-transform infrared spectroscopy, and transmission electron microscopy (TEM)) revealed that the synthesized MCM-41 has mesoporous characteristics: a high surface area and large pore volumes. The CO₂ adsorption capacity of MCM-41 and commercial nano-SiO₂ increased considerably with increasing CO₂ concentration and temperature, peaking at 60 °C. Below 60 °C, dynamics rather than thermodynamics governed the adsorption. Increasing the temperature from 60 to 80 °C decreased the adsorption capacity, and the reaction became thermodynamically dominant. Additionally, compared with commercial nano-SiO₂, the MCM-41 sorbent demonstrated superior regenerability and thermal stability.

The use of catalytic membranes as microstructured reactors without a separative function has proved effective. High catalytic activity is possible with minimal mass transport resistances if the reactant mixture is pushed to flow through the pores of a membrane that has been impregnated with catalyst. In this study, n-heptane (C₇H₁₆) was hydrocracked and hydro-isomerized within a plug-flow zeolitic catalytic membrane-packed bed reactor. The metallic cobalt (Co) precursor at 3 wt.% was loaded onto support mesoporous materials MCM-48 to synthesize heterogeneous catalysis. The prepared MCM-48 was characterized by utilizing characterization techniques such as scanning electron microscopy (SEM), X-ray diffraction (XRD), energy dispersive X-ray analysis (EDAX), Fourier transform infrared (FTIR), nitrogen adsorption–desorption isotherms, and the Brunauer–Emmett–Teller (BET) surface area. The structural and textural characteristics of MCM-48 after encapsulation with Co were also investigated. The analyses were performed before and after metal loading. According to the results, the 3 wt.% Co/MCM-48 of metallic catalyst in a fixed bed membrane reactor (MR) appears to have an excellent catalytic activity of ~83% during converting C₇H₁₆ at 400 °C, whereas a maximum selectivity was approximately ~65% at 325 °C. According to our findings, the synthesized catalyst exhibits an acceptable selectivity to isomers with multiple branches, while making low aromatic components. In addition, a good catalytic stability was noticed for this catalyst over the reaction. Use of 3 wt.% Co/MCM-48 catalyst led to the highest isomerization selectivity as well as n-heptane conversion. Therefore, the heterogeneous catalysis MCM-48 is a promising option/ alternative for traditional hydrocracking and hydro-isomerization processes.

Forward osmosis (FO) is a low-energy treatment process driven by osmosis to induce the separation of water from dissolved solutes/foulants through the membrane in hydraulic pressure absence while retaining all of these materials on the other side. All these advantages make it an alternative process to reduce the disadvantages of traditional desalination processes. However, several critical fundamentals still require more attention for understanding them, most notably the synthesis of novel membranes that offer a support layer with high flux and an active layer with high water permeability and solute rejection from both solutions at the same time, and a novel draw solution which provides low solute flux, high water flux, and easy regeneration. This work reviews the fundamentals controlling the FO process performance such as the role of the active layer and substrate and advances in the modification of FO membranes utilizing nanomaterials. Then, other aspects that affect the performance of FO are further summarized, including types of draw solutions and the role of operating conditions. Finally, challenges associated with the FO process, such as concentration polarization (CP), membrane fouling, and reverse solute diffusion (RSD) were analyzed by defining their causes and how to mitigate them. Moreover, factors affecting the energy consumption of the FO system were discussed and compared with reverse osmosis (RO). This review will provide in-depth details about FO technology, the issues it faces, and potential solutions to those issues to help the scientific researcher facilitate a full understanding of FO technology.

In this work, MXene as a hydrophilic 2D nanosheet has been suggested to tailor the polyphenylsulfone (PPSU) flat sheet membrane characteristics via bulk modification. The amount of MXene varied in the PPSU casting solution from 0–1.5 wt.%, while a series of characterization tools have been employed to detect the surface characteristics changes. This included atomic force microscopy (AFM), scanning electron microscopy (SEM), contact angle, pore size and porosity, and Fourier-transform infrared spectroscopy (FTIR). Results disclosed that the MXene content could significantly influence some of the membranes’ surface characteristics while no effect was seen on others. The optimal MXene content was found to be 0.6 wt.%, as revealed by the experimental work. The roughness parameters of the 0.6 wt.% nanocomposite membrane were notably enhanced, while greater hydrophilicity has been imparted compared to the nascent PPSU membrane. This witnessed enhancement in the surface characteristics of the nanocomposite was indeed reflected in their performance. A triple enhancement in the pure water flux was witnessed without compromising the retention of the membranes against the Cu²⁺, Cd²⁺ and Pd²⁺ feed. In parallel, high, and comparable separation rates (>92%) were achieved by all membranes regardless of the MXene content. In addition, promising antifouling features were observed with the nanocomposite membranes, disclosing that these nanocomposite membranes could offer a promising potential to treat heavy metals-containing wastewater for various applications.

Polyphenylsulfone (PPSU) membranes are critical for numerous applications, including water treatment, oil separation, energy production, electronic manufacturing, and biomedicine because of their low cost; regulated crystallinity; and chemical, thermal, and mechanical stability. Numerous studies...

Fuel cells have lately received growing attention since they allow the use of non-precious metals as catalysts, which reduce the cost per kilowatt of power in fuel cell devices to some extent. Until recent years, the major barrier in the development of fuel cells was the obtainability of highly conductive anion exchange membranes (AEMs). On the other hand, improvements show that newly enhanced anion exchange membranes have already reached high conductivity levels, leading to the suitable presentation of the cell. Currently, an increasing number of studies have described the performance results of fuel cells. Much of the literature reporting cell performance is founded on hydrogen‒anion exchange membrane fuel cells (AEMFCs), though a growing number of studies have also reported utilizing fuels other than hydrogen—such as alcohols, non-alcohol C-based fuels, and N-based fuels. This article reviews the types, performance, utilized membranes, and operational conditions of anion exchange membranes for fuel cells.

The emergence of mixed matrix membranes (MMMs) or nanocomposite membranes embedded with inorganic nanoparticles (NPs) has opened up a possibility for developing different polymeric membranes with improved physicochemical properties, mechanical properties and performance for resolving environmental and energy-effective water purification. This paper presents an overview of the effects of different hydrophilic nanomaterials, including mineral nanomaterials (e.g., silicon dioxide (SiO₂) and zeolite), metals oxide (e.g., copper oxide (CuO), zirconium dioxide (ZrO₂), zinc oxide (ZnO), antimony tin oxide (ATO), iron (III) oxide (Fe2O3) and tungsten oxide (WO_X)), two-dimensional transition (e.g., MXene), metal–organic framework (MOFs), covalent organic frameworks (COFs) and carbon-based nanomaterials (such as carbon nanotubes and graphene oxide (GO)). The influence of these nanoparticles on the surface and structural changes in the membrane is thoroughly discussed, in addition to the performance efficiency and antifouling resistance of the developed membranes. Recently, GO has shown a considerable capacity in wastewater treatment. This is due to its nanometer-sized holes, ultrathin layer and light and sturdy nature. Therefore, we discuss the effect of the addition of hydrophilic GO in neat form or hyper with other nanoparticles on the properties of different polymeric membranes. A hybrid composite of various NPs has a distinctive style and high-quality products can be designed to allow membrane technology to grow and develop. Hybrid composite NPs could be used on a large scale in the future due to their superior mechanical qualities. A summary and future prospects are offered based on the current discoveries in the field of mixed matrix membranes. This review presents the current progress of mixed matrix membranes, the challenges that affect membrane performance and recent applications for wastewater treatment systems.

A developed polydimethylsiloxane (PDMS) membrane was used to separate soluble benzene compounds (C₆H₆) from an aqueous solution via a pervaporation (PV) process. This membrane was characterized by scanning electron microscopy (SEM), Fourier-transform infrared (FTIR) spectroscopy, contact angle (CA), and energy-dispersive spectroscopy (EDS). To evaluate the performance of the membrane, the separation factor and permeation flux were estimated in various operating conditions, including the feed temperature, initial benzene concentration, and feed flow rate. The experiments to maximize the separation factor and permeation flux were designed using the response surface method (RSM) that is built into Minitab 18. A quadratic model (nonlinear regression equation) was suggested to obtain mathematical expressions to predict the benzene permeation flux and the separation factor according to the effect of the parameters’ interaction. The optimization of the PV was performed using an RSM that was based on the analysis of variance (ANOVA). The optimal values of the benzene permeation flux and separation factor were 6.7 g/m²·h and 39.8, respectively, at the optimal conditions of temperature (30 °C), initial concentration of benzene (1000 ppm), and feed flow rate (3.5 L/min). It was found that the feed concentration was the most influential parameter, leading to a significant increase in the permeation flux and separation factor of the PDMS membrane.