CDI crosslinked chitosan/poly (vinyl alcohol) electrospun nanofibers loaded with Achillea millefolium and Viola extract: A promising wound dressing.

Biopolymer-based electrospun mats, mimicking the extracellular matrix, have been extensively explored in biomedical applications. This study compares Achillea millefolium (AM) and Viola (V) extracts for developing a biocompatible wound dressing. The extracts were incorporated into a Chitosan/polyvinyl alcohol (CS/PVA) matrix via electrospinning. Crosslinking with Carbonyldiimidazole (CDI) improved chemical stability, water resistance, and biodegradability. The resulting mats exhibited flawless interconnected nanofibers, confirming the presence of AM and Viola extracts as analyzed via FTIR. Significant differences were observed between these two herbal extracts, particularly in mechanical properties, with tensile strengths of 6.9 MPa for AM and 17.2 MPa for Viola. Viola extract demonstrated robust antibacterial properties, producing an 8.2 mm inhibition zone against Staphylococcus aureus, compared to AM's 30 %. The release of therapeutic agents indicated an initial rapid phase, followed by a controlled 72 h release at a consistent rate. Notably, Viola extract led to 80.9 % wound closure on the 10th day, surpassing AM extract at 63.7 %. In contrast, the control group achieved only 32.1 % closure. This comparative study underscores the distinct advantages of AM and Viola extracts in wound dressing applications. While AM presents specific strengths, Viola extract exhibits superior mechanical properties, antibacterial efficacy, and accelerated wound closure, suggesting its potential with significant clinical implications.

Tailoring polyethylene oxide-modified cross-linked chitosan/PVA nanofibrous membranes: Burn dressing scaffold developed for mupirocin release.

In emergency treatment research, the focus on chitosan-based products for wound healing has been consistent. This study specifically explores a dressing made by mixing chitosan (CS) and poly (vinyl alcohol) PVA. Using electrospinning technology, nanofiber membranes of CS and PVA are created with the assistance of non-toxic and hydrophilic polyethylene oxide (PEO). The outcome is a new nanofibrous membrane loaded with mupirocin, designed for healing burn wounds. The study delves into the influence of PVA, CS, and PEO concentrations on the structural and chemical characteristics of the mats. This comprehensive exploration involves techniques such as Scanning Electron Microscope (SEM), Atomic Force Microscopy (AFM) imaging, Fourier Transform Infrared Spectrometry (FTIR analysis), and Contact angle measurements. Additionally, the research evaluates the antibacterial performance and biomedical behavior of the developed scaffolds. PEO proves beneficial in the electrospinning process, contributing to smoother fibers. Meanwhile, the addition of CS and mupirocin leads to formation of the thinner nanofibers (251 ± 5 µm and 263 ± 4 µm, respectively) and scaffolds with higher swelling (up to ∼3.5 times at 90 min). Notably, the (MTT) assay confirms the non-cytotoxicity of the fabricated nanofibers, with proliferations exceeding ∼85% for all samples. The crosslinked samples released the drug more slowly than the non-crosslinked dressings, with 80% of the scaffolds releasing the drug within 24 h. The in-vivo investigations suggested that the drug-containing scaffolds performed reliably and showed promise as a medical dressing for treating burn wounds.

A bilayer mupirocin/bupivacaine-loaded wound dressing based on chitosan/poly (vinyl alcohol) nanofibrous mat: Preparation, characterization, and controlled drug release.

An infected skin wound caused by external injury remains a serious challenge. Electrospun drug-loaded nanofibers with antibacterial properties based on biopolymers have been widely explored for wound healing. In this study, the double-layer CS/PVA/mupirocin (CPM) + CS/PVA/bupivacaine (CPB) mats were prepared by electrospinning method (20 % polymer weight) and then crosslinked with glutaraldehyde (GA) to optimize the water-resistant and biodegradation properties for wound dressing applications. The morphology of mats was characterized as defect-free and interconnected nanofibers by Scanning Electron Microscope (SEM) and Atomic Force Microscopy (AFM). Fourier Transform Infrared Spectrometry (FTIR) analysis also assessed the chemical structural properties. The porosity, surface wettability, and swelling degree of the dual-drug loaded mats were improved by about 20 %, 12°, and 200 % of the CS/PVA sample to provide a moist environment for efficient wound breathing and repairing. This highly porous mat facilitated the wound exudates absorption and air permeability excellently, reducing the chance of bacterial infections by inhibiting the growth of S. aureus bacterial colonies with a zone of 71.3 mm diameter. In vitro drug release results showed a high-burst release of 80 % and a continuous release profile for bupivacaine and mupirocin, respectively. MTT assay and in vivo tests indicated >90 % of cell viability and improvement in cell proliferation. It triply accelerated wound closure compared to the control group, reaching nearly full closure after 21 days as a potential clinical wound treatment.

Evaluation of process condition impact on copper and lead ions removal from water using goethite incorporated nanocomposite ultrafiltration adsorptive membranes.

Polyacrylonitrile (PAN) adsorptive membrane incorporated with nanosize-goethite (α-FeO(OH)) hydrous metal oxide particles (GNPs), prepared with optimal flux and Cu(II) removal in the previous study, was used to evaluate the process parameter on the Cu(II) removal. Box-Behnken Design (BBD) based on the Response Surface Methodology (RSM) was employed to evaluate the impact of Cu(II) feed solution characteristics such as pH, initial concentration of metal ion, and transmembrane pressure (TMP) on copper removal efficiency. The outcomes indicated that the RSM optimization technique could be utilized as an applicable method to find the optimum condition for the maximum Cu(II) removal with slight variance compared with the experimentally measured data. The effect of each process parameter and the coupling effect of parameters on the Cu(II) removal was assessed. Finally, the optimum condition of pH, Cu(II) concentration, and transmembrane pressure (TMP) to obtain high copper removal efficiency was decided. In the optimum condition of the Cu(II) removal, the removal of lead (Pb(II)) metal ion was evaluated by the same membrane.

One-Step and Low-Cost Designing of Two-Layered Active-Layer Superhydrophobic Silicalite-1/PDMS Membrane for Simultaneously Achieving Superior Bioethanol Pervaporation and Fouling/Biofouling Resistance.

Recently, the coupling of biofuel fermentation broths and pervaporation has been receiving increasing attention. Some challenges, such as the destructive effects of constituents of the real fermentation broth on the membrane performances, the lethal effects of the membrane surface chemical modifiers on the microorganisms, and being expensive, are against this concept. For the first time, a continuous study on the one-step and low-cost preparation of superhydrophobic membranes for bioethanol separation is made to address these challenges. In our previous work, spraying as a fast, scalable, and low-cost procedure was applied to fabricate the one-layered active-layer hydrophobic (OALH) silicalite-1/polydimethylsiloxane (PDMS) membrane on the low-cost mullite support. In this work, the spraying method was adopted to fabricate a two-layered active-layer superhydrophobic (TALS) silicalite-1/PDMS membrane, where the novel active layer consisted of two layers with different hydrophobicities and densities. Contact-angle measurements, surface charge determination, scanning electron microscopy, atomic force microscopy, and pervaporation separation using a 5 wt % ethanol solution were used to statically evaluate the fouling/biofouling resistance and pervaporation performances of OALH and TALS membranes in this study. The TALS membrane presented a better resistance and performance. For dynamic experiments, the Box-Behnken design was used to identify the effects of substrates, microorganisms, and nutrient contents as the leading indicators of fermentation broth on the TALS membrane performances for the long-term utilization. The maximum performances of 1.88 kg/m2·h, 32.34, and 59.04 kg/m2·h concerning the permeation flux, separation factor, and pervaporation separation index were obtained, respectively. The dynamic fouling/biofouling resistance of the TALS membrane was also characterized using energy-dispersive X-ray spectroscopy of all the tested membranes. The TALS membrane demonstrated the synergistic resistance of membrane fouling and biofouling. Eventually, the novel TALS membrane was found to have potential for biofuel recovery, especially bioethanol.

One-dimensional graphene for efficient aqueous heavy metal adsorption: Rapid removal of arsenic and mercury ions by graphene oxide nanoribbons (GONRs).

There is a knowledge gap for the application of one-dimensional graphene in the adsorption process. Our hypothesis was based on the fact that graphene oxide nanoribbons (GONRs) as one-dimensional graphene with more desired edges and specific surface area than other carbonaceous nanomaterials have more oxygen containing functional groups (active sites) on their edges and basal planes and therefore are more capable in adsorption of pollutants. In this regard, we synthesized GONRs by unzipping of multi-walled carbon nanotubes (MWCNTs) and investigated the adsorption behavior of GONRs by ultrasonic-assisted adsorptive removal of As(V) and Hg(II) ions from aqueous solution. The obtained results showed that As(V) ions are more favorably adsorbed onto the GONRs than Hg(II) ions and with increasing initial As(V) and Hg(II) ions concentration to 300 ppm, the equilibrium adsorption uptake of the synthesized GONRs increases to 155.61 and 33.02 mg/g for As(V) and Hg(II) ions, respectively through a rapid separation process in just 12 min. Also, three kinetic models and Freundlich and Langmuir adsorption isotherms were applied to evaluate the obtained experimental results. Our findings highlight the potential application of GONRs as one-dimensional graphene adsorbent with more desired edges than MWCNTs and graphene oxide (GO) and high adsorption capacity for selective removal of heavy metals.

Bio-inspired anchoring of amino-functionalized multi-wall carbon nanotubes (N-MWCNTs) onto PES membrane using polydopamine for oily wastewater treatment.

The major problem that limits the utilization of PES membranes in treatment of oily wastewater is the drastic irreversible membrane fouling due to the attachment of oil droplets onto the membrane surface. The goal of this study was to develop a novel, fast and facile post-functionalization of polydopamine (PDA) coated membranes using pre-synthesized nanoparticles for fabrication of novel organic-inorganic hybrid recoverable membranes with high hydrophilicity and underwater oleophobicity. Here, bio-inspired technique was studied because the membrane technology could separate small oil droplets (even <10 µm) with high performance if faced little fouling phenomena during the treatment process. The amino-functionalized multi-wall carbon nanotubes (N-MWCNTs) were anchored onto the PDA coated PES membranes. The membranes characteristics, with specific focus on surface morphology and wettability were investigated. The newly developed PES/PDA/N-MWCNTs membranes showed an enhanced flux (~1086%) compared to the unmodified PES membrane. This enhancement was attributed to the high hydrophilic and underwater oleophobic properties, which were found to alleviate the effect of fouling. The total fouling ratio (Rt) of the PES/PDA/N-MWCNTs membrane was 22.35%, which was far lower than that of the unmodified PES membrane (98.38%). Meanwhile, most of the fouling was reversible for the former with the remaining (irreversible fouling) of 18.08%. It was concluded that cake filtration is the dominant fouling mechanism of the PES/PDA/N-MWCNTs membranes due to their average pore diameter. The modified membranes showed high oil rejection (>99%) so that the obtained clean water with oil concentration lower than 5 ppm met the wastewater discharge standard recommendations. Also, evaluation of the PES/PDA/N-MWCNT membrane in cross-flow filtration showed its antifouling properties in the long-term application (16 h).

Assessing biomimetic aquaporin membrane for forward osmosis desalination process: A dataset.

This paper presents the performance of aquaporin forward osmosis membrane using chemical fertilizers as a draw solution. The comprehensive evaluation conducted for five conventional fertilizers ((CO (NH2)2, KCl, CaCl2, (NH4)2SO4) and (NH4)2HPO4) as draw solutions. The diluted fertilizer can be used directly for farming as fertigation. In this process, DSs do not need to be recovered and it is a single step desalination process. The data include the characterization of the intrinsic properties of the membrane samples and their performance under FO and PRO modes of operations. In addition, the data for various draw solution concentration under feed solution with deferent total dissolved solids (TDS) were evaluated. For example, a water flux of 17.5 L m- 2 h- 1 and 23.92 g m-2 h-1 reverse solute flux (RSF) was achieved under the FO operation mode for 3 M KCl.

Assessing the Binding Performance of Amyloid-Carbon Membranes toward Heavy Metal Ions.

Amyloid-carbon hybrid membranes have exceptional performance in removing heavy metal ions from water because of the presence of multiple binding sites on the amyloid fibrils, but the binding process is still not fully understood. To understand the mechanisms of amyloid-metal ion binding, we perform adsorption isotherms on a model system given by ß-lactoglobulin amyloid fibrils and four representative heavy metal ions: chromium (Cr), nickel (Ni), silver (Ag), and platinum (Pt). Furthermore, to get a comprehensive thermodynamic picture of the binding process between amino acid residues and heavy metals, we here use isothermal titration calorimetry on native ß-lactoglobulin monomers and amyloid fibrils exposed to the two model metal ions, that is, silver and chromium. A conclusive thermodynamic insight on the binding process emerges by direct measurements of enthalpy and entropy changes, association binding constant, and average number of binding sites of the protein monomer and amyloid fibril. As a result of the strong amyloid binding affinity between amino acids and metal ions, when the protein is converted into amyloid fibrils and assembled into membranes, the resulting amyloid-activated carbon hybrids remove all the tested heavy metals with efficiencies beyond 99%. Importantly, the efficiency remains stable during several consecutive cycles, demonstrating a high adsorption capacity and a long lifetime and reusability of the membranes. The recovery of adsorbed precious metal ions converted into elemental metals is shown to be a general feature of these membranes, with platinum and silver successfully recovered from saturated hybrid membranes by a simple thermal reduction. The separation performance, evaluated on real electroplating industrial wastewater containing chromium and nickel, is found to exceed 99% at a permeability as high as 2.92 × 10-16 m2, that is, at least 4 orders of magnitude higher than typical nanofiltration membranes, conclusively validating the technology under stringent real conditions.

Wastewaters treatment containing phenol and ammonium using aerobic submerged membrane bioreactor.

Phenolic wastewater was treated using anaerobic submerged membrane bioreactor (ASMBR). Effect of different solids retention times on MBR performance was studied. Various ratios of carbon to nitrogen were used in the synthetic wastewaters. During the operation, phenol concentration of feed was changed from 100 to 1000 mg L-1. Phenol concentration was increased stepwise over the first 30 days and kept constant at 1000 mg L-1, thereafter. For the first 100 days, a chemical oxygen demand (COD) to N ratio of 100:5.0 was used and this resulted in phenol and COD removal more than 99 and 95%, respectively. However, the ammonium removal decreased from 95 to 40% by increasing the phenol concentration of feed, from 100 to 1000 mg L-1. For the last 25 days, a COD to N ratio of 100:2.1 was used due to the ammonium accumulation in the ASMBR. This led to the complete ammonium removal and no ammonium was detected in the ASMBR permeate. These results suggest that in the ASMBR at high phenol loading of 1000 mg L-1, COD to N ratio of the phenolic wastewater must be 100:2.1 for ammonium removal, while at low phenol loading, COD to N ratio of 100:5.0 can be used.

Effect of hydrophobic and hydrophilic nanoparticles loaded in D2EHPA/M2EHPA - PTFE supported liquid membrane for simultaneous cationic dyes pertraction.

Cationic dyes mixture pertraction experiments of Rhodamine B (RhB) and Methylene Blue (MB) using a flat sheet supported liquid membrane (SLM) were performed. Mono-(2-etylhexyl) ester of phosphoric acid (M2EHPA) and bis-(2-etylhexyl) ester of phosphoric acid (D2EHPA) mixture was used as carrier and Sesame oil to dilute the carrier due to its very high viscosity. Acetic acid (AA) was also used as stripper phase. Influences of hydrophobic and hydrophilic nanoparticles were loaded in a carrier at different loadings (from 0 to 6 mg mL-1) on dyes pertraction at constant operating conditions were investigated. It was found that hydrophilic nanoparticles, including ZnO and TiO2 decrease dyes pertraction, while hydrophobic nanoparticles, including ZIF-8 and Fe3O4 favorably increase this parameter. ZIF-8 was found as the most effective nanoparticles on increasing dyes pertraction and the optimum loading was 2 mg mL-1. Also, the important process parameters that influence on the dyes mixture pertraction efficiency such as feed concentration, carrier concentration, feed pH and strip concentration were studied. In order to investigate the effects of operating parameters, all experiments were performed at a constant 2 mg mL-1 ZIF-8 loading. Optimum pertraction efficiency of RhB and MB were 90.6 and 79.4%, respectively. They were obtained after 10 h pertraction at optimum experimental conditions with feed concentration of 100 mg L-1, carrier concentration of 35% (vol), strip concentration of 0.5 mol L-1, and feed pH of 6. Effect of time on pertraction efficiencies at the optimum conditions were also studied.

Adsorption of divalent heavy metal ions from water using carbon nanotube sheets.

Removal of some divalent heavy metal ions (Cu(2+), Zn(2+), Pb(2+), Cd(2+), Co(2+)) from aqueous solutions using carbon nanotube (CNT) sheets was performed. CNT sheets were synthesized by chemical vapor deposition of cyclohexanol and ferrocene in nitrogen atmosphere at 750°C, and oxidized with concentrated nitric acid at room temperature and then employed as adsorbent for water treatment. Langmuir and Freundlich isotherms were used to describe the adsorption behavior of heavy metal ions by oxidized CNT sheets. The obtained results demonstrated that the oxidized CNT sheets can be used as an effective adsorbent for heavy metal ions removal from water. It was found out that kinetics of adsorption varies with initial concentration of heavy metal ions. Preference of adsorption onto the oxidized CNT sheets can be ordered as Pb(2+)>Cd(2+)>Co(2+)>Zn(2+)>Cu(2+). Using the oxidized CNT sheets, waste water treatment without CNT leakage into water is economically feasible. Therefore, CNT sheets have good potential application in environmental protection.