State-of-the-Art Polymer Science and Technology in Saudi Arabia (2021,2022)

Sodium borohydride (SBH) hydrolysis in the presence of cheap and efficient catalysts has been proposed as a safe and efficient method for generating clean hydrogen energy for use in portable applications. In this work, we synthesized bimetallic NiPd nanoparticles (NPs) supported on poly(vinylidene fluoride-co-hexafluoropropylene) nanofibers (PVDF-HFP NFs) via the electrospinning approach and reported an in-situ reduction procedure of the NPs being prepared by alloying Ni and Pd with varying Pd percentages. The physicochemical characterization provided evidence for the development of a NiPd@PVDF-HFP NFs membrane. The bimetallic hybrid NF membranes exhibited higher H₂ production as compared to Ni@PVDF-HFP and Pd@PVDF-HFP counterparts. This may be due to the synergistic effect of binary components. The bimetallic Ni_1−xPd_x(x = 0, 0.05, 0.1, 0.15, 0.2, 0.25, 0.3)@PVDF-HFP nanofiber membranes exhibit composition-dependent catalysis, in which Ni₇₅Pd₂₅@PVDF-HFP NF membranes demonstrate the best catalytic activity. The full H₂ generation volumes (118 mL) were obtained at a temperature of 298 K and times 16, 22, 34 and 42 min for 250, 200, 150, and 100 mg dosages of Ni₇₅Pd₂₅@PVDF-HFP, respectively, in the presence of 1 mmol SBH. Hydrolysis utilizing Ni₇₅Pd₂₅@PVDF-HFP was shown to be first order with respect to Ni₇₅Pd₂₅@PVDF-HFP amount and zero order with respect to the [NaBH₄] in a kinetics study. The reaction time of H₂ production was reduced as the reaction temperature increased, with 118 mL of H₂ being produced in 14, 20, 32 and 42 min at 328, 318, 308 and 298 K, respectively. The values of the three thermodynamic parameters, activation energy, enthalpy, and entropy, were determined toward being 31.43 kJ mol⁻¹, 28.82 kJ mol⁻¹, and 0.057 kJ mol⁻¹ K⁻¹, respectively. It is simple to separate and reuse the synthesized membrane, which facilitates their implementation in H₂ energy systems. Full article

The successful support of bimetallic NiCo alloy nanoparticles (NPs) on poly(vinylidene fluoride-co-hexafluoropropylene) nanofibers (PVDF-HFP NFs) was achieved through electrospinning (ES) and in situ reduction. The synthesis and physicochemical characterization of Ni-Co@PVDF-HFP NFs with a range of bimetallic compositions (Ni_1−xCo_x, x = 0, 0.1, 0.3, 0.5, 0.7, 0.9, and 1) supported on PVDF-HFP NFs was undertaken. In comparison to their counterparts (Ni-PVDF-HFB and Co-PVDF-HFB), the bimetallic hybrid NF membranes demonstrated a significantly increased volume of H₂ generation from sodium borohydride (SBH). The high performance of bimetallic catalysts can be attributed mostly to the synergistic impact of Ni and Co. Among all fabricated catalysts, Ni_0.3Co_0.7@PVDF-HFP produced the highest H₂ production in a short time. The maximum generated H₂volume was 118 mL in 11.5, 9, 6, and 4.5 min at 298, 308, 318, and 328 K, respectively. Kinetic analyses showed that the hydrolysis process proceeded as a quasi-first-order reaction with respect to the amount of catalyst and as a zero-order reaction with respect to the concentration of SBH. Thermodynamics studies were also undertaken and the parameters were calculated as E_a, ΔS, and ΔH = 30.17 kJ/mol, 0.065 kJ/mol, and 27.57 kJ/mol K, respectively. The introduced NFs can be easily separated and reused, which facilitates their industrialization and commercialization applications in hydrogen storage systems. Full article

Metallic Co NPs@poly(vinylidene fluoride-co- hexafluoropropylene) nanofibers (PVFH NFs) were successfully synthesized with the help of electrospinning and in situ reduction of Co²⁺ ions onto the surface of PVFH membrane. Synthesis of PVFH NFs containing 10, 20, 30, and 40 wt% of cobalt acetate tetrahydrate was achieved. Physiochemical techniques were used to confirm the formation of metallic Co@PVFH NFs. High catalytic activity of Co@PVFH NFs in the dehydrogenation sodium borohydride (SBH) was demonstrated. The formulation with 40 wt% Co proved to have the greatest performance in comparison to the others. Using 1 mmol of SBH and 100 mg of Co@PVFH NFs, 110 mL of H₂ was produced in 19 min at a temperature of 25 °C, but only 56, 73, and 89 mL were produced using 10, 20, and 30 wt% Co, respectively. With the rise of catalyst concentration and reaction temperature, the amount of hydrogen generated increased. By raising the temperature from 25 to 55 °C, the activation energy was lowered to be 35.21 kJ mol⁻¹ and the yield of H₂ generation was raised to 100% in only 6 min. The kinetic study demonstrated that the reaction was pseudo-first order in terms of the amount of catalyst utilized and pseudo-zero order in terms of the SBH concentration. In addition, after six cycles of hydrolysis, the catalyst showed outstanding stability. The suggested catalyst has potential applications in H₂ generation through hydrolysis of sodium borohydride due to its high catalytic activity and flexibility of recycling. Full article

A transparent smart window made of recycled polycarbonate plastic (PCP) waste was prepared and immobilized with strontium aluminate phosphor nanoparticles (SAPN). It has afterglow emission, super-hydrophobicity, durability, photostability, good mechanical properties, ultraviolet protection, and high optical transmittance. To create an afterglow emission polycarbonate smart window (SAPN@PCP), recycled polycarbonate waste was integrated with various concentrations of SAPN (15–52 nm). SAP micro-scale powder was made using the solid-state high temperature method. The SAP nanoparticles were produced using the top-down method. To create a colorless plastic bulk, recycled polycarbonate waste was inserted into a hot bath. This colorless plastic was thoroughly combined with SAPN and cast to create an afterglow luminous smart window. To investigate its photoluminescence properties, spectrum profiles of excitation and emission were measured. According to the luminescence parameters, the phosphorescent colorless polycarbonate plates displayed a change in color to strong green under UV illumination and greenish-yellow in a dark box. The afterglow polycarbonate smart window displayed two emission peaks at 496 and 526 nm, and an absorption wavelength of 373 nm. Upon increasing the SAPN ratio, the hydrophobic activity, hardness, photostability, and UV protection were improved. Luminescent polycarbonate substrates with lower SAPN ratio demonstrated rapid and reversible fluorescence under UV light, while the higher SAPN content in the luminous polycarbonate substrates showed afterglow. Full article

In this study, cotton-reinforced alginate hydrogel fibers were successfully synthesized using the wet spinning technique to improve hydrogel fibers’ mechanical strength and durability. Structural, chemical, and mechanical properties of the prepared fibers were characterized using scanning electron microscopy, Fourier transform infrared spectroscopy, X-ray Diffraction, differential scanning calorimeter, and single fiber strength tester. Based on the results obtained from fourier transform infrared spectroscopy and x-ray Diffraction, cotton fibers have been successfully incorporated into the structure of the hydrogel fibers. It was seen from the differential scanning calorimeter results that the incorporation of fibers in the structure even enhanced the thermal stability of the fiber and is viable to be implanted in the human body. Cotton reinforcement in alginate hydrogel fibers increases the modulus up to 56.45 MPa providing significant stiffness and toughness for the hydrogel composite fiber. The tenacity of the fibers increased by increasing the concentration of alginate from 2.1 cN/Tex (1% w/v) to 8.16 cN/Tex (1.5% w/v). Fiber strength increased by 26.75% and water absorbance increased by 120% by incorporating (10% w/w) cotton fibers into the fibrous structure. It was concluded that these cotton-reinforced alginate hydrogel fibers have improved mechanical properties and liquid absorption properties suitable for use in various biomedical applications. Full article

In this study, the preparation of graphene oxide@chitosan (GO@CS) composite beads was investigated via continuous dropping techniques to remove methylene blue (MB)-dye from an aqueous media. The prepared beads were characterized using various techniques before and after the adsorption of MB. The experimental results showed that the adsorption processes fit the kinetic pseudo-second-order and Langmuir isotherm models. Moreover, the GO@CS beads achieve maximum adsorption capacities of 23.26 mg g⁻¹, which was comparable with other adsorbents in the literature. An important advantage of our adsorbent is that the GO@CS can remove 82.1% of the real sample color within 135 min. Full article

Fabrication of electrospun nanofibers based on the blending of modified natural polymer, hydroxyl propyl starch (HPS) as one of the most renewable resources, with synthetic polymers, such as polyurethane (PU) is of great potential for biomedical applications. The as-prepared nanofibers were used as antimicrobial sheets via blending with biosynthesized silver nanoparticles (AgNPs), which were prepared in a safe way with low cost using the extract of Nerium oleander leaves, which acted as a reducing and stabilizing agent as well. The biosynthesized AgNPs were fully characterized by various techniques (UV-vis, TEM, DLS, zeta potential and XRD). The obtained results from UV-vis depicted that the AgNPs appeared at a wavelength equal to 404 nm affirming the preparation of AgNPs when compared with the wavelength of extract (there are no observable peaks). The average particle size of the fabricated AgNPs that mediated with HPS exhibited a very small size (less than 5 nm) with excellent stability (more than −30 mv). In addition, the fabricated nanofibers were also fully characterized and the obtained data proved that the diameter of nanofibers was enlarged with increasing the concentration of AgNPs. Additionally, the findings illustrated that the pore sizes of electrospun sheets were in the range of 75 to 350 nm. The obtained results proved that the presence of HPS displayed a vital role in decreasing the contact angle of PU nanofibers and thus, increased the hydrophilicity of the net nanofibers. It is worthy to mention that the prepared nanofibers incorporated with AgNPs exhibited incredible antimicrobial activity against pathogenic microbes that actually presented in human wounds. Moreover, P. aeruginosa was the most sensitive species to the fabricated nanofibers compared to other tested ones. The minimal inhibitory concentrations (MICs) values of AgNPs-3@NFs against P. aeruginosa, and E. faecalis, were 250 and 500 mg/L within 15 min, respectively. Full article

Tertiary oil recovery, commonly known as enhanced oil recovery (EOR), is performed when secondary recovery is no longer economically viable. Polymer flooding is one of the EOR methods that improves the viscosity of injected water and boosts oil recovery. Xanthan gum is a relatively cheap biopolymer and is suitable for oil recovery at limited temperatures and salinities. This work aims to modify xanthan gum to improve its viscosity for high-temperature and high-salinity reservoirs. The xanthan gum was reacted with acrylic acid in the presence of a catalyst in order to form xanthan acrylate. The chemical structure of the xanthan acrylate was verified by FT-IR and NMR analysis. The discovery hybrid rheometer (DHR) confirmed that the viscosity of the modified xanthan gum was improved at elevated temperatures, which was reflected in the core flood experiment. Two core flooding experiments were conducted using six-inch sandstone core plugs and Arabian light crude oil. The first formulation—the xanthan gum with 3% NaCl solution—recovered 14% of the residual oil from the core. In contrast, the modified xanthan gum with 3% NaCl solution recovered about 19% of the residual oil, which was 5% higher than the original xanthan gum. The xanthan gum acrylate is therefore more effective at boosting tertiary oil recovery in the sandstone core. Full article

In the present study, cylindrical ABS P400 polymer parts (diameter 6.5 mm) to be used as die-sinking EDM (electric discharge machining) novel electrodes were fabricated using a fused deposition modeling (FDM) process. To meet the conductivity requirement in EDM, ABS parts were metallized using an innovative method that comprised putting aluminum–charcoal (Al–C) on them followed by their copper electroplating. Real-time EDM of the mild steel workpiece was performed using novel electrodes, and machining performance of the electrodes, measured in terms of dimensional accuracy, i.e., change in diameter (ΔD) and change in depth (ΔH) of the cavity, under varying levels of three EDM factors, i.e., current (I), pulse on time (T_on), and pulse off time (T_off), was investigated. Machining results were analyzed using analysis of variance (ANOVA), perturbation graphs, and 3D surface plots. The optimal setting of the EDM parameters for minimizing ΔD and ΔH was determined using the desirability function approach. The suitability of the novel electrodes for EDM was ascertained by comparing their machining results with those of solid copper (SC) electrodes and electrodes fabricated by FDM and metallized using the electro-deposition method (FDM-EM), already reported in the literature, under similar machining conditions. From the results, it was found that ΔD and ΔH were less when EDM was performed using novel electrodes. Full article

Hydrogels wound dressings have enormous advantages due to their ability to absorb high wound exudate, capacity to load drugs, and provide quick pain relief. The use of hydrogels as wound dressings in their original form is a considerable challenge, as these are difficult to apply on wounds without support. Therefore, the incorporation of polymeric hydrogels with a certain substrate is an emerging field of interest. The present study fabricated cellulose hydrogel using the sol–gel technique and reinforced it with nonwoven cotton for sustainable wound dressing application. The nonwoven cotton was immersed inside the prepared solution of cellulose and heated at 50 °C for 2 h to form cellulose hydrogel–nonwoven cotton composites and characterized for a range of properties. In addition, the prepared hydrogel composite was also loaded with titania particles to attain antibacterial properties. The Fourier transform infrared spectroscopy and scanning electron microscopy confirmed the formation of cellulose hydrogel layers inside the nonwoven cotton structure. The fabricated composite hydrogels showed good moisture management and air permeability, which are essential for comfortable wound healing. The wound exudate testing revealed that the fluid absorptive capacity of cellulose hydrogel nonwoven cotton composite was improved significantly in comparison to pure nonwoven cotton. The results reveal the successful hydrogel formation, having excellent absorbing, antimicrobial, and sustainable properties. Full article

Green enhanced oil recovery (GEOR) is an eco-friendly EOR technique involving the injection of specific green fluids to improve macroscopic and microscopic sweep efficiencies, boosting residual oil production. The environmentally friendly surfactant-polymer (SP) flood is successfully tested in a sandstone reservoir. However, the applicability of the SP method does not extend to carbonate reservoirs yet and requires comprehensive investigation. This work aims to explore the oil recovery competency of a green SP formulation in carbonate through experimental and modelling studies. Numerous formulations of SP with ketone, alcohol, and organic acid are selected based on phase behavior and interfacial tension (IFT) reduction capabilities to examine their potential for enhancing residual oil production from carbonate cores. A blending of nonionic green surfactant alkyl polyglucoside (APG), xanthan gum (XG) biopolymer, and butanone recovered 22% tertiary oil from the carbonate core. This formulation recovered more than double residual crude than that of the APG, XG, and acetone. Similarly, a combination of APG, XG, acrylic acid, and butanol increased significantly more oil than the APG, XG, and acrylic acid formulation. The APG, XG, and butanone mixture is efficient with regards to boosting tertiary oil recovery from the carbonate core. Full article

A series of UV-protected coatings were prepared using cerium-oxide-functionalized oil fly ash (f-OFA-CeO₂) in waterborne polyurethane (WBPU) dispersions. Three monomers, namely, poly(tetramethyleneoxide glycol) (PTMG), polydimethylsiloxane-hydroxy terminated (PDMS) and 4,4-dicyclohexylmethane diisocyanate (H₁₂MDI), were used to pre-mix with f-OFA-CeO₂ separately, followed by the synthesis of WBPU/f-OFA-CeO₂ dispersions. The f-OFA-CeO₂ distribution and enrichment into any part (top/bottom/bulk) of the coating was strongly affected by the pre-mixing of f-OFA-CeO₂. The f-OFA-CeO₂ was densely distributed in the top, bottom and bulk when the f-OFA-CeO₂ was pre-mixed with PDMS, H₁₂MDI and PTMG, respectively. Only an f-OFA-CeO₂-enriched top surface showed excellent UV protection. The lowest UV-degraded exposed coating was found when the top surface of the coating was f-OFA-CeO₂-enriched. Full article

Converting low-cost bio-plant residuals into high-value reusable nanomaterials such as microcrystalline cellulose is an important technological and environmental challenge. In this report, nanocrystalline cellulose (NCC) was prepared by acid hydrolysis of macrocrystalline cellulose (CEL). The newly synthesized nanomaterials were fully characterized using spectroscopic and microscopic techniques including FE-SEM, FT-IR, TEM, Raman spectroscopy, and BET surface area. Morphological portrayal showed the rod-shaped structure for NCC with an average diameter of 10–25 nm in thickness as well as length 100–200 nm. The BET surface area of pure CEL and NCC was found to be 10.41 and 27 m²/g, respectively. The comparative protection capacity of natural polymers CEL and NCC towards improving the SS316 alloy corrosion resistance has been assessed during the acid pickling process by electrochemical (OCP, PDP, and EIS), and weight loss (WL) measurements. The outcomes attained from the various empirical methods were matched and exhibited that the protective efficacy of these polymers augmented with the upsurge in dose in this order CEL (93.1%) < NCC (96.3%). The examined polymers display mixed-corrosion inhibition type features by hindering the active centers on the metal interface, and their adsorption followed the Langmuir isotherm model. Surface morphology analyses by SEM reinforced the adsorption of polymers on the metal substrate. The Density Functional Theory (DFT) parameters were intended and exhibited the anti-corrosive characteristics of CEL and NCC polymers. A Monte Carlo (MC) simulation study revealed that CEL and NCC polymers are resolutely adsorbed on the SS316 alloy surface and forming a powerful adsorbed protective layer. Full article

Hydraulic fracturing consumes massive volumes of freshwater that is usually scarce and costly. Such operation is not sustainable, and hence seawater could be used as an alternative. Nevertheless, seawater has high total dissolved solids (TDS), affecting the fracturing fluid rheology and providing a damage potential to the subterranean hydrocarbon reservoirs. Resolving these issues requires fracturing fluid systems with many additives, which results in an expensive and non-eco-friendly system. This study proposes eco-friendly and biodegradable chelating agents that could replace many additives such as scale inhibitors and crosslinkers. The study aims to optimize the rheology of seawater fracturing fluids using a chelating agent and polymer. By optimizing N,N-Dicarboxymethyl glutamic acid (GLDA) conditions, high viscosity was achieved using a standard industry rheometer. The GLDA was mixed with carboxymethyl hydroxypropyl guar (CMHPG) polymer and tested in both deionized water (DW) and seawater (SW). The polymer was examined first, where the rheology did not show a time-dependent behavior. The polymer in SW showed a slightly higher viscosity than in DW. The GLDA and CMHPG were tested at different temperatures, pH, and concentrations. These sets showed a time-dependent viscosity behavior, which can be utilized in various fracturing steps. Results showed that the solution pH and GLDA concentration significantly impacted the fluid viscosity magnitude and behavior. The developed formulation is shear thinning, where the viscosity declines as the shear rate increases. The temperature negatively impacted the viscosity and caused the formulation to break. The study provided an understanding of how to optimize the rheology of SW fracturing fluid based on GLDA chelating and CMHPG polymer. Full article

Green enhanced oil recovery is an oil recovery process involving the injection of specific environmentally friendly fluids (liquid chemicals and gases) that effectively displace oil due to their ability to alter the properties of enhanced oil recovery. In the microbial enhanced oil recovery (MEOR) process, microbes produce products such as surfactants, polymers, ketones, alcohols, and gases. These products reduce interfacial tension and capillary force, increase viscosity and mobility, alter wettability, and boost oil production. The influence of ketones in green surfactant-polymer (SP) formulations is not yet well understood and requires further analysis. The work aims to examine acetone and butanone’s effectiveness in green SP formulations used in a sandstone reservoir. The manuscript consists of both laboratory experiments and simulations. The two microbial ketones examined in this work are acetone and butanone. A spinning drop tensiometer was utilized to determine the interfacial tension (IFT) values for the selected formulations. Viscosity and shear rate across a wide range of temperatures were measured via a Discovery hybrid rheometer. Two core flood experiments were then conducted using sandstone cores at reservoir temperature and pressure. The two formulations selected were an acetone and SP blend and a butanone and SP mixture. These were chosen based on their IFT reduction and viscosity enhancement capabilities for core flooding, both important in assessing a sandstone core’s oil recovery potential. In the first formulation, acetone was mixed with alkyl polyglucoside (APG), a non-ionic green surfactant, and the biopolymer Xanthan gum (XG). This formulation produced 32% tertiary oil in the sandstone core. In addition, the acetone and SP formulation was effective at recovering residual oil from the core. In the second formulation, butanone was blended with APG and XG; the formulation recovered about 25% residual oil from the sandstone core. A modified Eclipse simulator was utilized to simulate the acetone and SP core-flood experiment and examine the effects of surfactant adsorption on oil recovery. The simulated oil recovery curve matched well with the laboratory values. In the sensitivity analysis, it was found that oil recovery decreased as the adsorption values increased. Full article

The objective of this study was to synthesize and assess unfilled and filled (silica nanoparticles) dentin adhesive polymer. Methods encompassing scanning electron microscopy (SEM)—namely, energy dispersive X-ray spectroscopy (EDX), micro-tensile bond strength (µTBS) test, Fourier transform infrared (FTIR), and micro-Raman spectroscopy—were utilized to investigate Si particles’ shape and incorporation, dentin bond toughness, degree of conversion (DC), and adhesive–dentin interaction. The Si particles were incorporated in the experimental adhesive (EA) at 0, 5, 10, and 15 wt. % to yield Si-EA-0% (negative control group), Si-EA-5%, Si-EA-10%, and Si-EA-15% groups, respectively. Teeth were set to form bonded samples using adhesives in four groups for µTBS testing, with and without aging. Si particles were spherical shaped and resin tags having standard penetrations were detected on SEM micrographs. The EDX analysis confirmed the occurrence of Si in the adhesive groups (maximum in the Si-EA-15% group). Micro-Raman spectroscopy revealed the presence of characteristic peaks at 638, 802, and 1300 cm⁻¹ for the Si particles. The µTBS test revealed the highest mean values for Si-EA-15% followed by Si-EA-10%. The greatest DC was appreciated for the control group trailed by the Si-EA-5% group. The addition of Si particles of 15 and 10 wt. % in dentin adhesive showed improved bond strength. The addition of 15 wt. % resulted in a bond strength that was superior to all other groups. The Si-EA-15% group demonstrated acceptable DC, suitable dentin interaction, and resin tag formation. Full article

Chitosan is broadly used as a biological material since of its excellent biological activities. This work describes investigations of chitosan interaction with SARS-CoV-2, which is occupied by human respiratory epithelial cells through communication with the human angiotension-converting enzyme II (ACE2). The β-chitosan derivatives are synthesized and characterized by FT-IR, nuclear magnetic resonance (¹H and ¹³C NMR), mass spectrometry, X-ray diffraction, TGA, DSC, and elemental analysis. The β-chitosan derivatives were screened for cytotoxic activity against the HepG2 and MCF-7 (breast) cancer cell lines. Compound 1h (GI₅₀ 0.02 µM) is moderately active against the HepG2 cancer cell line, and Compound 1c is highly active (GI₅₀ 0.01 µM) against the MCF-7 cancer cell line. In addition, chitosan derivatives (1a–1j) docking against the SARS coronavirus are found by in-silico docking analysis. The findings show that compound 1c exhibits notable inhibition ability compared with other compounds, with a binding energy value of −7.9 kcal/mol. Based on the molecular docking results, the chitosan analog is proposed to be an alternative antiviral agent for SARS-CoV2. Full article

Polysaccharide materials are widely applied in different applications including food, food packaging, drug delivery, tissue engineering, wound dressing, wastewater treatment, and bioremediation sectors. They were used in these domains due to their efficient, cost-effective, non-toxicity, biocompatibility, and biodegradability. As is known, polysaccharides can be synthesized by different simple, facile, and effective methods. Of these polysaccharides are cellulose, Arabic gum, sodium alginate, chitosan, chitin, curdlan, dextran, pectin, xanthan, pullulan, and so on. In this current article review, we focused on discussing the synthesis and potential applications of microbial polysaccharides. The biosynthesis of polysaccharides from microbial sources has been considered. Moreover, the utilization of molecular biology tools to modify the structure of polysaccharides has been covered. Such polysaccharides provide potential characteristics to transfer toxic compounds and decrease their resilience to the soil. Genetically modified microorganisms not only improve yield of polysaccharides, but also allow economically efficient production. With the rapid advancement of science and medicine, biosynthesis of polysaccharides research has become increasingly important. Synthetic biology approaches can play a critical role in developing polysaccharides in simple and facile ways. In addition, potential applications of microbial polysaccharides in different fields with a particular focus on food applications have been assessed. Full article

Hydrogen (H₂) is a promising renewable energy source that can replace fossil fuels since it can solve several environmental and economic issues. However, the widespread usage of H₂ is constrained by its storage and safety issues. Many researchers consider solid materials with an excellent capacity for H₂ storage and generation as the solution for most H₂-related issues. Among solid materials, ammonia borane (abbreviated hereafter as AB) is considered one of the best hydrogen storage materials due to its extraordinary H₂ content and small density. However, the process must be conducted in the presence of efficient catalysts to obtain a reasonable amount of generated H₂. Electrospun nanofibrous catalysts are a new class of efficient catalysts that involves the usage of polymers. Here, a comprehensive review of the ceramic-supported electrospun NF catalysts for AB hydrolysis is presented, with a special focus on catalytic and photolytic performance and preparation steps. Photocatalytic AB hydrolysis was discussed in detail due to its importance and promising results. AB photocatalytic hydrolysis mechanisms under light were also explained. Electrospun catalysts show excellent activity for AB hydrolysis with good recyclability. Kinetics studies show that the AB hydrolysis reaction is independent of AB concentration and the first-order reaction of NF catalysts. Full article