Publications by authors named "Ahmad Arabi Shamsabadi"

Mixed-matrix membranes (MMMs) with favorable interfacial interactions between dispersed and continuous phases offer a promising approach to overcome the traditional trade-off between permeability and selectivity in membrane-based gas separation. In this study, we developed free-standing MMMs by embedding pristine and surface-modified TiCT MXenes into Matrimid 5218 polymer for efficient CO/CH separation. Two-dimensional TiCT with adjustable surface terminations provided control over these critical interfacial interactions.

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  • * It finds that when the size of silica NPs decreases, both thermal degradation and photo-degradation rates of the molecular glasses also decrease significantly, enhancing their stability.
  • * The research indicates that extreme nanoconfinement slows down reaction product transport, leading to improved durability, suggesting potential applications in coatings and organic electronics.
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Integrating biocidal nanoparticles (NPs) into polyamide (PA) membranes shows promise for enhancing resistance to biofouling. Incorporating techniques can tailor thin-film nanocomposite (TFN) membranes for specific water purification applications. In this study, silver-based metal-organic framework Ag-MOFs (using silver nitrate and 1,3,5-benzentricarboxylic acid as precursors) are incorporated into PA membranes via three different methods: i) incorporation, ii) dip-coating, and iii) in situ ultrasonic techniques.

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The mutations of bacteria due to the excessive use of antibiotics, and generation of antibiotic-resistant bacteria have made the development of new antibacterial compounds a necessity. MXenes have emerged as biocompatible transition metal carbide structures with extensive biomedical applications. This is related to the MXenes' unique combination of properties, including multifarious elemental compositions, 2D-layered structure, large surface area, abundant surface terminations, and excellent photothermal and photoelectronic properties.

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When aged below the glass transition temperature, [Formula: see text], the density of a glass cannot exceed that of the metastable supercooled liquid (SCL) state, unless crystals are nucleated. The only exception is when another polyamorphic SCL state exists, with a density higher than that of the ordinary SCL. Experimentally, such polyamorphic states and their corresponding liquid-liquid phase transitions have only been observed in network-forming systems or those with polymorphic crystalline states.

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The effect of nanoporous confinement on the glass transition temperature () strongly depends on the type of porous media. Here, we study the molecular origins of this effect in a molecular glass, -bis(3-methylphenyl)--diphenylbenzidine (TPD), highly confined in concave and convex geometries. When confined in controlled pore glass (CPG) with convex pores, TPD's vibrational spectra remained unchanged and two 's were observed, consistent with previous studies.

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In this work, nanorods with high antibacterial properties were synthesized with silver acetate as the metal source and 2-aminoterephthalic acid as the organic linker and were then embedded into thin-film composite (TFC) membranes to amend their performance as well as to alleviate biofouling. Silver metal-organic framework (Ag-MOF) nanorods with a length smaller than 40 nm were incorporated within the polyamide thin selective layer of the membranes during interfacial polymerization. The interaction of the synthesized nanorods with the polyamide was favored because of the presence of amine-containing functional groups on the nanorod's surface.

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In this study, a polyamide forward osmosis membrane was functionalized with zwitterions followed by the in situ growth of metal-organic frameworks with silver as a metal core (Ag-MOFs) to improve its antibacterial and antifouling activity. First, 3-bromopropionic acid was grafted onto the membrane surface after its activation with ,-diethylethylenediamine. Then, the in situ growth of Ag-MOFs was achieved by a simple membrane immersion sequentially in a silver nitrate solution and in a ligand solution (2-methylimidazole), exploiting the underlying zwitterions as binding sites for the metal.

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  • Membranes combining TiCT MXene nanosheets with Pebax-1657 demonstrate outstanding CO separation efficiency, exceeding typical performance limits.
  • Characterization shows that strong hydrogen bonds between the materials create pathways for efficient CO transport.
  • The new membranes are not only easy to fabricate but also economically viable for energy-efficient CO capture at a cost of $29 per ton.
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  • Extreme nanoconfinement significantly enhances the thermal stability and reduces the flammability of polystyrene (PS) by infiltrating it into silica nanoparticle films.
  • As the size of the silica nanoparticles decreases, the thermal degradation time of PS increases up to 30 times at 543 K, with a notable rise in activation energy for degradation.
  • The degradation process is mostly limited by diffusion, occurring from the film surface inward and resulting in less char formation, while the overall dynamics of the nanoparticles remain similar to bulk materials.
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Poly(vinyl chloride) (PVC)/SiO nanocomposite hollow-fiber membranes with different nano-SiO particle loadings (0-5 wt %) were fabricated using the dry-jet wet-spinning technique. Effects of SiO nanoparticles on the morphology of the prepared hollow-fiber membranes were investigated using scanning electron microscopy. Transport and antifouling properties of the fabricated membranes were evaluated by conducting pure-water permeation, solute rejection, and fouling resistance experiments.

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  • Thin-film composite (TFC) membranes are prone to fouling and biofouling, which affects their performance.
  • Researchers developed a thin-film nanocomposite (TFN) membrane by adding graphene oxide (GO)-silver-based metal-organic framework (Ag-MOF), resulting in enhanced anti-biofouling and antifouling traits.
  • The new GO-Ag-MOF TFN membrane showed significantly improved water permeability and a higher ability to eliminate E. coli compared to other membrane types, demonstrating its superior effectiveness against fouling.
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This work shows that incorporating highly compatible polyrhodanine nanoparticles (PRh-NPs) into a polyamide (PA) active layer allows for fabricating forward osmosis (FO) thin-film composite (TFC)-PRh membranes that have simultaneously improved antimicrobial, antifouling, and transport properties. To the best of our knowledge, this is the first reported study of its kind to this date. The presence of the PRh-NPs on the surface of the TFC-PRh membranes active layers is evaluated using FT-IR spectroscopy, SEM, and XPS.

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In addition to possessing excellent chemical, mechanical, and thermal stability, polyimides and polyetherimides have excellent solubility in many solvents, which renders them suitable for membrane preparation. Two new monomers [a pentiptycene-based dianhydride (PPDAn) and a pentiptycene imide-containing diamine (PPImDA)] and a pentiptycene-based polyimide [PPImDA-4,4'-hexafluoroisopropylidene diphthalic anhydride (PPImDA-6FDA)] have been synthesized and characterized by FTIR and H NMR spectroscopy, gel-permeation chromatography, mass spectrometry, X-ray photoelectron spectroscopy, thermogravimetric analysis, differential scanning calorimetry, BET surface area, and X-ray diffraction. High-molecular-weight PPImDA-6FDA has remarkable thermal stability and excellent solubility in common organic solvents.

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  • This study explores the use of a silver-based metal-organic framework (MOF) to reduce biofouling in forward-osmosis thin-film composite membranes, marking the first investigation of MOFs for this purpose.
  • The MOF nanocrystals were successfully incorporated into the membrane's active layer during the polymerization process, enhancing properties like hydrophilicity and transport without compromising selectivity.
  • Results showed a significant reduction in bacterial attachment (over 90% less) and improved biofouling resistance, with only an 8% decline in membrane performance after 24 hours compared to a 21% decline for control membranes.
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The lattice of 5,7,12,14-tetra-hydro-5,14:7,12-bis-([1,2]benzeno)-penta-cene-6,13-dione, CHO, at 173 K has triclinic (-1) symmetry and crystallizes with four independent half-mol-ecules in the asymmetric unit. Each mol-ecule is generated from a CHO substructure through an inversion center at the centroid of the central quinone ring, generating a wide H-shaped mol-ecule, with a dihedral angle between the mean planes of the terminal benzene rings in each of the two symmetry-related pairs over the four mol-ecules of 68.6 (1) (), 65.

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Membrane adsorbents have emerged as powerful and attractive tools for the removal of hazardous materials such as dyes and heavy metal ions, mainly in trace amounts, from water resources. Among membrane adsorbents, those prepared from or modified with chitosan biopolymer and its derivatives are cases of interest because of chitosan advantages including biocompatibility, biodegradability, nontoxicity, reactivity, film and fiber forming capacity and favorable hydrophilicity. This review is oriented to provide a framework for better insight into fabrication methods and applications of chitosan-based adsorptive membranes.

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