Sorption induced relaxations during water diffusion in S-PEEK

This paper presents an analysis of the sorption kinetics of water vapor and liquid water in the glassy polymer sulfonated poly(ether ether ketone) (S-PEEK). Sorption isotherms are determined experimentally using a gravimetric sorption balance, and the relative contributions of Fickian diffusion and relaxational phenomena are quantified as a function of the water concentration in the polymer using the model of Hopfenberg and Berens.Analysis of the sorption isotherms and determination of the sorption kinetics prove the occurrence of both Fickian sorption behavior and relaxational phenomena already at very low water concentrations in the polymer. With increasing water concentration, the relative importance of relaxation phenomena increases, whereas the relative contribution of Fickian diffusion decreases.Based on the water vapor sorption kinetics only, the Fickian diffusion coefficient increases over two orders of magnitude with increasing water vapor concentration. Taking also the diffusion kinetics from liquid water sorption experiments into account reveals a change of even three orders of magnitude of the Fickian diffusion coefficient when the water concentration in the polymer increases

Electrospinning of sustainable polymers from biomass for active food packaging

<jats:p>This review outlines the latest developments in using electrospun materials derived from sustainable, biomass-sourced polymers for active food packaging applications.</jats:p&gt

Electrospinning of Cyclodextrin Functional Nanofibers for Drug Delivery Applications

Electrospun nanofibers have sparked tremendous attention in drug delivery since they can offer high specific surface area, tailored release of drugs, controlled surface chemistry for preferred protein adsorption, and tunable porosity. Several functional motifs were incorporated into electrospun nanofibers to greatly expand their drug loading capacity or to provide the sustained release of the embedded drug molecules. In this regard, cyclodextrins (CyD) are considered as ideal drug carrier molecules as they are natural, edible, and biocompatible compounds with a truncated cone-shape with a relatively hydrophobic cavity interior for complexation with hydrophobic drugs and a hydrophilic exterior to increase the water-solubility of drugs. Further, the formation of CyD-drug inclusion complexes can protect drug molecules from physiological degradation, or elimination and thus increases the stability and bioavailability of drugs, of which the release takes place with time, accompanied by fiber degradation. In this review, we summarize studies related to CyD-functional electrospun nanofibers for drug delivery applications. The review begins with an introductory description of electrospinning; the structure, properties, and toxicology of CyD; and CyD-drug complexation. Thereafter, the release of various drug molecules from CyD-functional electrospun nanofibers is provided in subsequent sections. The review concludes with a summary and outlook on material strategies

Electrospinning of Cyclodextrin Nanofibers: The Effect of Process Parameters

Cyclodextrin (CD) nanofibers have recently emerged as high-performance materials owing to their large surface area-to-volume ratio, along with the presence of high active CD content for their applications in drug delivery and water treatment. Even though there are several studies on the polymer-free electrospinning of CD molecules of different types, the effects of electrospinning process parameters on the morphology and diameter of the resultant fibers have not addressed yet. In this study, the influence of electrospinning process variables on the morphology and diameter of the resultant CD nanofibers is systematically studied using two different solvent systems, i.e., water and N, N-dimethylformamide (DMF). On adjusting the electrospinning process parameters (i.e., electrical field, flow rate, tip-to-collector distance (TCD), and needle diameter), uniform CD nanofibers could be produced from aqueous and DMF solutions. Generally, the electrospinning of thicker fibers was observed by increasing the applied voltage and flow rate due to higher mass flow. Increasing TCD boosted the fiber diameter. Likewise, the use of needles with larger diameters resulted in the electrospinning of thicker fibers from DMF solutions, which might be attributed to higher viscosity due to reduced shear rate

Influence of Hydrogen-Bonding Additives on Electrospinning of Cyclodextrin Nanofibers

The electrospinning of highly concentrated solutions of cyclodextrin (CD) leads to bead-free nanofibers without the need of a polymeric carrier. The occurrence of numerous hydrogen bonds among CD molecules is the main driving force for their electrospinning, and hence, additives with hydrogen-bonding potential can disturb the aggregation of CD molecules and affect their electrospinning. In this study, we systematically investigated the influence of five different hydrogen-bonding additives, i.e., methylamine (MA), ethylenediamine (ED), urea, 2,2,2-trifluoroethanol (TFE), and 1,1,1,3,3,3-hexafluoroisopropanol (HFIP), on the solution behavior of hydroxypropyl-β-CD (HP-β-CD) by rheology, conductivity, and NMR analyses, and the morphology of the electrospun HP-β-CD nanofibers by scanning electron microscopy. The 1H NMR chemical shifts of the HP-β-CD protons in D2O were observed with the incorporation of hydrogen-bonding molecules due to the occurrence of intermolecular associations between HP-β-CD and additives. Dynamic light scattering measurements revealed a clear decrease in the aggregate size with the introduction of additives. Unlike other additives, which showed a general decreasing trend in viscosity with increasing additive content, the addition of MA led to a significant increase in the viscosity with increasing concentration and gave rise to HP-β-CD nanofibers at lower concentrations. The addition of low concentrations of ED, urea, TFE, and HFIP led to thinner nanofibers due to the lower viscosity of the respective solutions. Increasing additive content deteriorated the electrospinnability of HP-β-CD solutions, resulting in beaded fibers. A systematic relationship was found between the solution viscosity and morphology of the respective electrospun fibers. Overall, this study, for the first time, reports the influence of hydrogen bonding on the polymer-free electrospinning of CD molecules and shows a correlation between solution properties and morphology of their electrospun nanofibers

Cyclodextrin-assisted synthesis of tailored mesoporous silica nanoparticles

Mesoporous silica nanoparticles (MSNs) have sparked considerable interest in drug/gene delivery, catalysis, adsorption, separation, sensing, antireflection coatings and bioimaging because of their tunable structural properties. The shape, size and pore structure of MSNs are greatly influenced by the type of additives used, e.g., solvent and pore-templating agent. Here, we studied the influence of cyclodextrin (CD) molecules on the formation of MSNs. The nanoparticles over 100 nm in diameter were synthesized by surfactant-templated, hydrolysis–polycondensation reactions in the presence of pristine CD (β-CD) or hydroxypropyl-functionalized CDs (HP-γ-CD and HP-β-CD). Depending on the formulation conditions, differently shaped MSNs, such as bean-like, spherical, ellipsoid, aggregate and faceted were generated. The morphology and size of MSNs varied with the CD-type used. Generally, spherical particles were obtained with β-CD, while a faceted morphology was observed for the particles synthesized using HP-CDs. The particle size could be tuned by adjusting the amount of CD used; increasing the CD concentration led to larger particles. MSNs synthesized in the presence of β-CD displayed a smaller particle size than those produced with HP-functional CDs. FTIR, TGA and solid-state 13C NMR demonstrated the adsorption of CDs on the particle surfaces. The proposed concept allows for the synthesis of silica nanoparticles with control over particle shape and size by adjusting the concentration of additives in a simple, one-pot reaction system for a wide range of applications

Electrospinning of uniform nanofibers of Polymers of Intrinsic Microporosity (PIM-1): The influence of solution conductivity and relative humidity

WOS: 000483922700023Polymers of Intrinsic Microporosity (PIMs) are ultra-permeable macromolecules, which can be cast as a dense membrane and exploited in a wide spectrum of applications, particularly for gas separation owing to their extremely large inner surface area, free volume and high gas permeability. While they are mostly intended to serve as membranes for gas separation, in recent years, they have been also employed in water treatment applications owing to their solution processability, which enables the production of fibrous membranes by electrospinning. The fibrous form provides an increase in sorption performance, water permeability and flux for their application in water treatment. However, owing to the low conductivity of PIM-1 solutions in 1,1,2,2-tetrachloroethane (TeCA) that is the ideal solvent for the electrospinning of PIM-1 solutions, a higher polymer concentration is required to produce bead-free fibers. Furthermore, the electrospinning of highly concentrated PIM-1 solutions leads to the formation of microfibers. To tackle these problems, we herein incorporated an ammonium salt (i.e., tetraethylammonium bromide, TEAB) to increase the conductivity of PIM-1 solutions and study the impact of solution conductivity on the electrospinning of PIM-1 solutions. In parallel to the conductivity study, the influence of relative humidity on the electrospinning and morphology of PIM-1 fibers was explored. The addition of TEAB significantly increased the solution conductivity and drastically enhanced the electrospinnability of PIM-1. The electrospinning of PIM-1 solutions (10% (w/v)) in the presence 7.5 wt% TEAB (with respect to PIM-1) led to bead-free fibers, while at the same concentration, electrosprayed beads and droplet splashing were observed in the absence of TEAB. On the other hand, increasing humidity did not influence the electrospinnability of PIM-1 and the fiber texture, however, less fibers were formed in a given time at very high humidity conditions (similar to 80%). Overall, the experimental findings revealed that the addition of the salt drastically enhanced the electrospinnability of PIM-1 solutions owing to the enhanced conductivity and could lead to the formation of very thin PIM-1 fibers with 160 nm in diameter while no significant effect of relative humidity on the electrospinnability of PIM-1 solutions was observed

Efficient Removal of Polycyclic Aromatic Hydrocarbons and Heavy Metals from Water by Electrospun Nanofibrous Polycyclodextrin Membranes

Here, a highly efficient membrane based on electrospun polycyclodextrin (poly-CD) nanofibers was prepared and exploited for the scavenging of various polycyclic aromatic hydrocarbons (PAHs) and heavy metals from water. The poly-CD nanofibers were produced by the electrospinning of CD molecules in the presence of a cross-linker (i.e., 1,2,3,4-butanetetracarboxylic acid), followed by heat treatment to obtain an insoluble poly-CD nanofibrous membrane. The membrane was used for the removal of several PAH compounds (i.e., acenaphthene, fluorene, fluoranthene, phenanthrene, and pyrene) and heavy metals (i.e., Pb2+, Ni2+, Mn2+, Cd2+, Zn2+, and Cu2+) from water over time. Experiments were made on the batch sorption of PAHs and heavy metals from contaminated water to explore the binding affinity of PAHs and heavy metals to the poly-CD membrane. The equilibrium sorption capacity (qe) of the poly-CD nanofibrous membrane was found to be 0.43 ± 0.045 mg/g for PAHs and 4.54 ± 0.063 mg/g for heavy metals, and the sorption kinetics fitted well with the pseudo-second-order model for both types of pollutants. The membrane could be recycled after treatment with acetonitrile or a 2% nitric acid solution and reused up to four times with similar performance. Further, dead-end filtration experiments showed that the PAH removal efficiencies were as high as 92.6 ± 1.6 and 89.9 ± 4.8% in 40 s for the solutions of 400 and 600 μg/L PAHs, respectively. On the other hand, the removal efficiencies for heavy metals during the filtration were 94.3 ± 5.3 and 72.4 ± 23.4% for 10 and 50 mg/L solutions, respectively, suggesting rapid and efficient filtration of heavy metals and PAHs by the nanofibrous poly-CD membrane

Sorption induced relaxations during water diffusion in S-PEEK

\u3cp\u3eThis paper presents an analysis of the sorption kinetics of water vapor and liquid water in the glassy polymer sulfonated poly(ether ether ketone) (S-PEEK). Sorption isotherms are determined experimentally using a gravimetric sorption balance, and the relative contributions of Fickian diffusion and relaxational phenomena are quantified as a function of the water concentration in the polymer using the model of Hopfenberg and Berens. Analysis of the sorption isotherms and determination of the sorption kinetics prove the occurrence of both Fickian sorption behavior and relaxational phenomena already at very low water concentrations in the polymer. With increasing water concentration, the relative importance of relaxation phenomena increases, whereas the relative contribution of Fickian diffusion decreases. Based on the water vapor sorption kinetics only, the Fickian diffusion coefficient increases over two orders of magnitude with increasing water vapor concentration. Taking also the diffusion kinetics from liquid water sorption experiments into account reveals a change of even three orders of magnitude of the Fickian diffusion coefficient when the water concentration in the polymer increases.\u3c/p\u3