Increase In Water Contact Angle Research Articles

Construction of a durable, halogen-free, and phosphorus-free flame retardant cotton fabric system with hydrophobic properties by phase separation and interface polymerization

Inspired by the synthesis of polyurethane, a multifunctional fabric with hydrophobic and long-lasting flame retardancy was prepared through the phase separation and interfacial reaction process between PEI (polyethyleneimine)/BX (borax) aqueous solution and isocyanate terminated polydimethylsiloxane (PDMS-NCO) in tetrahydrofuran solution. The limit oxygen index of the treated fabric increased from 18.0 % to 33.7 %, and the total heat release decreased by 34.2 %. The enhancement of flame retardant performance and thermal stability is attributed to the enhanced char-forming capacity. After 50 cycles of water washing, the cotton fabric can still pass the vertical flammability test because of the curing effect of PDMS-NCO on functional additives. Furthermore, SEM analysis revealed that the formation of nano-rough structures on the fibers was promoted by phase separation, thus leading an increased water contact angle of sample to 139°. The materials utilized in this modified process do not contain elements such as F, Cl, Br, and P, indicating its potential as an environmentally friendly methodology for fabric functionalization.

Antimicrobial guar gum films optimized with Pickering emulsions of zein-gum arabic nanoparticle-stabilized composite essential oil for food preservation

In this study, composite essential oil Pickering emulsion stabilized with zein-gum arabic (GA) nanoparticles (ZGCEO) was prepared to improve the characteristics of guar gum (GG) films. ZGCEO exhibited commendable stability and compatibility with GG, while leading to a noticeable improvement in the light barrier (from 3.98 A mm−1 to 17.09 A mm−1) and water vapor barrier characteristics of GG films, concomitantly mitigating their hydrophilic nature, with decreasing moisture content (from 17.70 % to 10.50 %), water solubility (from 84.41 % to 71.79 %), water vapor permeability (from 5.64 × 10−11 g (m s Pa)−1 to 4.97 × 10−11 g (m s Pa)−1), and an increasing water contact angle (from 69.8° to 94.2°). The addition of 2 % ZGCEO yielded a notable increase in the tensile strength of the GG-ZGCEO films, but the elongation at break decreased with increasing ZGCEO concentration. Moreover, the incorporated ZGCEO demonstrated outstanding antioxidant and antimicrobial characteristics, featuring a slow-release behavior of essential oil. The GG-ZGCEO coating also showed an excellent preservation effect in pork and “Huangguan” pears during storage. Collectively, we substantiated the efficacy of ZGCEO in augmenting the functional attributes of GG films, thereby establishing their potential utility as antimicrobial packaging materials conducive to food preservation.

Fabrication and characterization of an alginate-based film incorporated with cinnamaldehyde for fruit preservation

Sodium alginate (SA) is widely used in the food, biomedical, and chemical industries due to its biocompatibility, biodegradability, and excellent film-forming properties. This article introduces a simple method for preparing uniform alginate-based packaging materials with exceptional properties for fruit preservation. The alginate was uniformly crosslinked by gradually releasing calcium ions triggered by the sustained hydrolysis of gluconolactone (GDL). A cinnamaldehyde (CA) emulsion, stabilized by xanthan without the use of traditional surfactants, was tightly incorporated into the alginate film to enhance its antimicrobial, antioxidant, and UV shielding properties. The alginate-based film effectively blocked ultraviolet rays in the range of 400–200 nm, while allowing for a visible light transmittance of up to 70 %. Additionally, it showed an increased water contact angle and decreased water vapor permeability. The alginate-based film was also employed in the preparation of coated paper through the commonly used coating process in the papermaking industry. The alginate-based material displayed excellent antioxidant properties and antimicrobial activity against Escherichia coli, Staphylococcus aureus and Botrytis cinerea, successfully extending the shelf life of strawberries to 7 days at room temperature. This low-cost and facile method has the potential to drive advancements in the food and biomedical fields by tightly incorporating active oil onto a wide range of biomacromolecule substrates.

Study on multi‐cycle gas‐water displacing mechanism in underground gas storage of low‐permeability reservoir based on PNM

AbstractA deep understanding of the pore‐scale multi‐cycle two‐phase seepage mechanism of gas‐water systems in low‐permeability reservoirs is crucial for enhancing oil and gas recovery and optimizing the operating conditions of underground gas storage. A pore network model was reconstructed using micro‐CT images of low‐permeability core samples from the Dagang Oilfield, China. The mathematical models of gas‐water flow in the pore‐scale models were established based on Poiseuille's law and the quasi‐static displacement theory, considering the gas compressibility and slip effects. The porosity, pore size, absolute permeability, and relative permeability (Kr) of oil‐water and gas‐water were calculated using pore network simulations and validated against experimental benchmark data of the same samples. The effects of multi‐cycle displacement, rock wettability, and average pore pressure on the gas‐water two‐phase flow were simulated and analyzed. The results showed that the relative permeability of gas (Krg) at the same water saturation level significantly increased when the gas compressibility and slip effects were considered. With an increase in the number of gas‐water displacement cycles, Krg at the same water saturation level showed a decreasing trend, indicating a reduction in the gas seepage capability. Krg decreased with increasing water contact angle. With an increase in the average pore pressure, Krg decreased and gradually increased when the average pressure exceeded 25 MPa.

Development of cellulose/ZnO based bioplastics with enhanced gas barrier, UV-shielding effect and antibacterial activity

Development of renewable and biodegradable plastics with good properties, such as the gas barrier, UV-shielding, solvent resistance, and antibacterial activity, remains a challenge. Herein, cellulose/ZnO based bioplastics were fabricated by dissolving cellulose carbamate in an aqueous solution of NaOH/Zn(OH)42−, followed by coagulation in aqueous Na2SO4 solution, and subsequent hot-pressing. The carbamate groups detached from cellulose, and ZnO which transformed from cosolvent to nanofiller was uniformly immobilized in the cellulose matrix during the dissolution/regeneration process. The appropriate addition of ZnO (below 10.67 wt%) not only improved the mechanical properties but also enhanced the water and oxygen barrier properties of the material. Additionally, our cellulose/ZnO based bioplastic demonstrated excellent UV-blocking capabilities, increased water contact angle, and enhanced antibacterial activity against S. aureus and E. coli, deriving from the incorporation of ZnO nanoparticles. Furthermore, the material exhibited resistance to organic solvents such as acetone, THF, and toluene. Indeed, the herein developed cellulose/ZnO based bioplastic presents a promising candidate to replace petrochemical plastics in various applications, such as plastic toys, anti-UV guardrails, window shades, and oil storage containers, offering a combination of favorable mechanical, gas barrier, UV-blocking, antibacterial, and solvent-resistant properties.

Effect of zirconia coating on Ti6Al4V at elevated substrate temperature on its wear, corrosion and hemocompatibility properties

Titanium and its alloys have been recognized as biocompatible materials since decades although these materials can at times show wear, corrosion and thrombosis leading to various health complications. Surface coating has been found to be one of the effective techniques to overcome this issue in-vitro as well as in-vivo. In this paper, thin film coating of zirconia (ZrO2) on Ti6Al4V is reported using pulsed laser deposition (PLD) technique at elevated substrate temperatures ranging from room temperature to 800 °C (TiZr800). The morphology, composition, wettability and average surface roughness of the samples were analyzed by scanning electron microscope, Raman spectrometer, water contact angle (WCA) and profilometer, respectively. Adhesion between film and substrate was qualified using Elcometer. The tribological studies were performed in ball-on-disc against ZrO2 counterpart, the electrochemical potential analysis was done in simulated body fluid to replicate body environment and the hemocompatibility test was evaluated on the basis of human whole blood adsorption and distribution of Red Blood Cells (RBCs) on the samples. The results revealed an increase in WCA and film adhesion with increased substrate temperature. At 800 °C, formation of zirconium carbide, a relatively harder material, was observed due to diffusion of substrate carbon into ZrO2 film, as confirmed by the Raman analysis. In comparison to pristine, TiZr800 sample showed a reduction in wear rate from 3.5 × 10−3 mm3/Nm to 1.1 × 10−3 mm3/Nm indicating improved resistance of the sample against abrasive wear. Further, drop in Icorr from 4.96 × 10−7 A/cm2 to 2.75 × 10−7 A/cm2 resulted in a 44 % increase in corrosion protective efficiency of the sample coated at 800 °C. Additionally, a 4.5 fold increase in RBC counts was observed on TiZr800 sample. Therefore, it is inferred that while ZrO2 coating can improve overall surface properties of Ti–6Al–4V, additional benefits can be obtained by performing PLD at higher substrate temperatures, more so when the temperature is such as to promote formation of ZrC in the coating.

Highly water-resistant paper via infiltration with polymeric microspheres from nanocellulose-stabilized plant oil-derived monomer

Sustainable strategies to improve the water resistance of cellulose paper are actively sought. In this work, polymeric microspheres (PMs), prepared through emulsion polymerization of cellulose nanofibers stabilized rubber seed oil-derived monomer, were investigated as coatings on corrugated medium paper (CMP). After infiltrating porous paper with PMs, the water-resistant corrugated papers (WRCPn) with enhanced mechanical properties were obtained. When 30 wt% PMs were introduced, WRCP30 turned out to be highly compacted with an increased water contact angle of 106.3° and a low water vapor transmission rate of 81 g/(m2 d) at 23 °C. Meanwhile, the tensile strength of WRCP30 increased to 22.2 MPa, a 4-fold increase from CMP. When tested in a well-hydrated state, 71% of its mechanical strength in the dry state was maintained. Even with a low content of 10 wt% PMs, WRCP10 also exhibited stable tensile strength and water wettability during the cyclic soaking-drying process. Thus, the plant oil based sustainable emulsion polymers provide a convenient route for enhancing the overall performance of cellulose paper.

Ion-bombardment-driven surface modification of porous magnesium scaffolds: Enhancing biocompatibility and osteoimmunomodulation

Porous Mg scaffolds are promising for bone repair but are limited by high corrosion rates and challenges in preserving coating integrity. We used Directed Plasma Nanosynthesis (DPNS) at 400 eV and a fluence of 1 × 1018 cm−2 to augment the bioactivity and corrosion resistance of porous Mg scaffolds, maintaining their overall material integrity. DPNS creates nanostructures that increase surface area, promote apatite nucleation, and enhance osseointegration, improving the bioactivity and corrosion resistance of porous Mg scaffolds without compromising their structure. Our findings indicate a decrease in surface roughness, with pre-irradiated samples having Rq = 60.4 ± 5.3 nm andRa = 48.2 ± 3.1 nm, and post-DPNS samples showing Rq = 36.9 ± 0.3 nm andRa = 28.6 ± 0.8 nm. This suggests changes in topography and wettability, corroborated by the increased water contact angles (CA) of 129.2 ± 3.2 degrees. The complexity of the solution influences the CA: DMEM results in a CA of 120.4 ± 0.1 degrees, while DMEM + SBF decreases it to 103.6 ± 0.5 degrees, in contrast to the complete spreading observed in non-irradiated samples. DPNS-treated scaffolds exhibit significantly reduced corrosion rates at 5.7 × 10−3 ± 3.8 × 10−4 mg/cm²/day, compared to the control's 2.3 × 10−2 ± 3.2 × 10−4 mg/cm²/day over 14 days (P < 0.01). The treatment encourages the formation of a Ca-phosphate-rich phase, which facilitates cell spreading and the development of focal adhesion points in hBM-MSCs on the scaffolds. Additionally, J774A.1 murine macrophages show an enhanced immune response with diminished TNF-α cytokine expression. These results offer insights into nanoscale modifications of Mg-based biomaterials and their promise for bone substitutes or tissue engineering scaffolds.

Development of an edible food packaging gelatin/zein based nanofiber film for the shelf-life extension of strawberries.

An edible food packaging gelatin/zein nanofiber film co-loaded with cinnamaldehyde (CA)/thymol (THY) was developed, which possessed outstanding features conducive to strawberries preservation. Firstly, the synergistic antibacterial behavior of CA and THY was investigated. Then CA and THY were co-loaded into gelatin/zein nanofiber films by electrospinning technology. The addition of CA and THY increased water contact angle to 85.1° after 10s and decreased the water vapor transmission rate of 3.1×10-8 g·mm-1·h-1·Pa-1. The tensile strength was 1.30MPa and the elongation at break was 185%. The nanofiber films exhibited good shielding effect of ultraviolet-visible light and excellent antioxidant capacity with DPPH free radical scavenging percentage of 99.9% in 4h. The nanofiber films (12.5mg/mL) could achieve significant inhibition effects on Escherichia coli ATCC 25922 with the bacteriostatic ratio of 67.5%, Staphylococcus aureus ATCC 6538 and Listeria monocytogenes ATCC 19115 with the antibacterial ratios of 100%. A real-time study on the nanofiber films as fruit packaging materials was carried out on strawberries and the packaged strawberries kept their freshness as long as 7days at room temperature. Therefore, the GZ/CT nanofiber film prepared in this work has good application potential in the field of fruit packaging.

Constructing a biodegradable carrageenan based food packaging film according to the synergistic strategies between peppermint essential oil and thymol

The research and development trend of food packaging is changing from synthetic polymers to eco-friendly materials such as polysaccharides and other hydrocolloids, aiming to solve the problem of pollution from plastic wastes. In this work, a biodegradable food packaging noted KC/PT film was constructed using konjac glucomannan (KGM)/carrageenan (CAR) composite as the matrix and peppermint essential oil (PO)/thymol (THY) with synergistic effect as the reinforcements. The KC/PT film showed great mechanical properties, UV-blocking activity, increased water contact angle and reduced water vapor permeability. Due to the synergistic effect between PO and THY, the KC/PT film showed excellent antioxidant performance and antibacterial behavior against Escherichia coli ATCC 25922, Listeria monocytogenes ATCC 19115 and Staphylococcus aureus ATCC 6538. The antibacterial mechanism was further illustrated. The prepared KC/PT film, as a unique packaging film, not only successfully extended the shelf life of strawberry to 16 days at 4 °C, but also well expressed its environmental friendliness that it could nearly degrade after 47 days in natural soil conditions. Most importantly, the film exhibited good stability in terms of mechanical properties, antioxidant activity and antibacterial performances after 4 months storage. Therefore, the film the KC/PT film has great potentials in the field of food packaging area.

Engineering biodegradable controlled gelatin-zein bilayer film with improved mechanical strength and flexibility

Compiling hydrophobic and hydrophilic proteins to form mechanically reliable bilayer film with improved water barrier properties and hydrophobicity to replace petroleum-based standards is challenging because fabricating compatible surfaces and flexible film with interlinked interfaces is complex. The mechanical properties of gelatin and zein layers exhibited unique variations, and synergistic enhancement of bilayer properties reflected robust layer-by-layer (LBL) interactions. To overcome the problem of impaired integrated surface, viscously cross-linked zein film forming solution (FFS) by glyoxal (GX) introduced compact and closely entangled network formation with cross-linking of gelatin film. Zein surface compatibility and flexibility by GX and polyethylene glycol (PEG 400) synergized with the gelatin layer closed to compare flexible plastic materials such as PE and PP besides modulated color and transparency. Enhancing flexible formation was mechanized by acetic acid as solvent of zein solution after long-range repulsion during casting on well-manageable plasticized and cross-linked gelatin film with glutaraldehyde (GA) and PEG 400, respectively. Elongation (E%) was achieved by nearly 192% with modified tensile strength (TS) and Young's modulus (YM). Cross-linkers, especially GX, resulted in lower water solubility (WS), and joint layers resulted in controlled water vapor permeability (WVP) of bilayer films. Decreased surface roughness and WS increased water contact angle (WCA). FTIR spectroscopy, XRD analysis, DMTA, and SDS-PAGE analyzed cross-linking mode and intensity. Hence, gelatin-zein bilayer films showed significant potential for improving value-added functional properties.

Physicochemical and antioxidant properties of tannic acid crosslinked cationic starch/chitosan based active films for ladyfinger packaging application

In the present study, cationic starch (CS)/chitosan (CH) incorporated with tannic acid (TA)(CSCT) eco-friendly films were prepared by employing an inexpensive solvent casting technique. Influence of TA on the physicochemical and antimicrobial properties of CS/CH polymer matrix were studied. The FTIR findings and homogeneous, dense SEM micrographs confirms the effective interaction of TA with CS/CH polymer matrix. CSCT-3 active film displayed tensile strength of 26.99±1.91 MPa, which is more substantial than commercially available polyethylene (PE) (12–16 MPa) films. The active films exhibited excellent barrier properties against moisture and water, supported by increased water contact angle values (86.97±0.29°). Overall migration rate of active films was found to be below the permitted limit of 10mg/dm2. The active films showed around 56% of degradation in soil within 15 days. Besides, the active films showed concurring impact against food borne pathogens like E. coli, S. aureus and C. albicans. The CSCT-3 active film presented 90.83% of antioxidant capacity, demonstrating the effective prevention of food oxidation related deterioration. Ladyfinger packaging was inspected to examine the ability of active films as packaging material resulted in effectively resisting deterioration and extending shelf life in comparison with traditional PE packaging.

Alkyl ketene dimer modification of thermomechanical pulp promotes processability with polypropylene

AbstractAlkyl ketene dimers (AKDs) are known to efficiently react with cellulose with a dual polarity in their structure: a polar component and a nonpolar component. AKD of three different carbon chain lengths, 4, 10, and 16 carbons have been synthesized, and thermomechanical pulp (TMP) fibers were modified by them. The modification of TMP fibers with AKD resulted in an increased water contact angle, showing the presence of the AKDs on the TMP fibers and a new carbonyl peak in the IR spectra, suggesting modification of the TMP fibers with AKD groups. Calculating the Hansen solubility parameters of AKD and AKD conjugated to TMP in polypropylene (PP) indicates improved compatibility, especially of longer chain AKD and TMP AKD. The rheological studies of the composites showed that the AKD with the longest carbon chain decreases the melt viscosity of the PP‐TMP‐AKD composite, which combined with the shape and the color of the extruded composite filaments indicates improved flow properties and reduced stress build up during processing. The research findings demonstrate the ability of AKD to enhance the dispersibility and compatibility of natural fibers with PP.

Enhanced Lifetime of Cyanine Salts in Dilute Matrix Luminescent Solar Concentrators via Counterion Tuning.

Organic luminophores offer great potential for energy harvesting and light emission due to tunable spectral properties, strong luminescence, high solubility, and excellent wavelength-selectivity. To realize their full potential, the lifetimes of luminophores must extend to many years under illumination. Many organic luminophores, however, have a tendency to degrade and undergo rapid photobleaching, leading to the perception of intrinsic instability of organic molecules. In this work we demonstrate that by exchanging the counterion of a heptamethine cyanine salt the photostability and corresponding lifetime of dilute cyanine salts can be enhanced by orders of magnitude from 10 hours to an extrapolated lifetime of greater than 65,000 hours under illumination. To help correlate and comprehend the underlying mechanism behind this phenomenon, the water contact angle and binding energy of each pairing were measured and calculated. We find that increased water contact angle, and therefore increasing hydrophobicity, generally correlate to improved lifetimes. Similarly, a lower absolute binding energy between cation and anion correlates to increased lifetimes. Utilizing the binding energy formalism, we predict the stability of a new anion and experimentally verify with good consistency. Moving forward, these factors could be used to rapidly screen and identify highly photostable organic luminophore salt systems for a range of energy harvesting and light emitting applications.

Dispersion of hydrophobic waste amorphous carbon powder in cementitious environment and its effect on the permeability of cement paste

A Proper dispersion of powder-based hydrophobic admixtures in cementitious composites is challenging due to the presence of water. Studies have shown that amorphous carbon powder (ACP), a hydrophobic by-product of refining waste materials of paraffin production can be used as a hydrophobic agent. However, mixing methods and dispersing agents for modifying cementitious materials with ACP can significantly impact their mechanical properties, workability, water-repellency (hence the durability), and dispersion quality of ACP. Lack of information about the extent of their impact on different aspects mentioned above can hinder the practical use of ACP as a hydrophobic agent. To fill this gap, the objective of this study is to comprehensively investigate factors in the dispersion of ACP in cementitious materials and the tradeoff between mechanical properties and water permeability of ACP-modified cementitious materials when more than one mixing method is adopted. The impacts of different dispersing agents and mixing methods, including ultrasonication, dry mixing, and after mixing, on dispersion quality of ACP in cementitious environment analogous with aqueous solutions and hardened cement paste were assessed. Polycarboxylate ether-based superplasticizer (PCE) proved to be the most effective dispersing agent. Compressive strength of ACP modified cement paste can be increased or decreased with or without the workability reduction effect of ACP along with PCE respectively. Based on volume fraction of ACP clusters in X-ray micro-CT 3D reconstruction of hardened cement paste, ultrasonication was identified as the most effective mixing method and dry mixing was the worst in terms of achieving a uniform distribution of ACP in cement paste. However, all mixing methods presented more than 85% volume fraction of uniformly dispersed ACP areas with no major difference in terms of hydrophobic modification capability. Modifying cement paste with a higher amounts of ACP (5 to 15% by weight of cement) substantially increased water contact angle (up to 171% for w/c ratio of 0.35) and decreased water absorption. The hydrophobic modification capability of ACP increases with a decrease in the quality of cement paste and is diminished by the presence of PCE. Consequently, without PCE, water absorption rate was reduced by up to 92% in similar ACP modified cement paste samples, which also led to a major reduction in compressive strength.

Effects of functionalization and silane modification of hexagonal boron nitride on thermal/mechanical/morphological properties of silicon rubber nanocomposite

Hexagonal boron nitride (h-BN) nanoparticles could induce interesting properties to silicone rubber (SR) but, the weak filler-matrix interfacial interaction causes agglomeration of the nanoparticles and declines the performance of the nanocomposite. In this work, h-BN nanoparticles were surface modified using vinyltrimethoxysilane (VTMS) at different concentrations. Before silane modification, h-BN nanoparticles were hydroxylated using 5 molar sodium hydroxide. The nanoparticles were characterized to assess success of silane grafting. The pure and modified h-BN nanoparticles were applied at 1, 3 and 5 wt% to HTV silicon rubber (SR). The curing, thermal, mechanical and morphological properties and hydrophobicity of the nanocomposites were evaluated. The morphology of the SR nanocomposites was characterized using AFM and FE-SEM analysis. It was found that silane grafting on the h-BN nanoparticles improves crosslink density but declines curing rate index (CRI) of the SR nanocomposite (at 5 wt% loading content) by 0.7 (dN m) and 3.5%, respectively. It also increased water contact angle of the nanocomposites from 97.5° to 107°. The improved nanoparticle-rubber interfacial interactions caused better dispersion of h-BN nanoparticles in SR matrix (at 5 wt%) that enhanced the elongation at break, modulus at 300% and Tg of the SR nanocomposites.

Influence of surface characteristics of cement pavement on ice-concrete adhesion

Breaking the adhesion between ice- and pavement is crucial for road de-icing. This study investigates the impact of concrete pavement surface characteristics on ice-pavement adhesion. To achieve this, 20 cement concrete specimens with different combinations of 10 surface textures and 2 wettability surface characteristics were prepared. The water contact angle (WCA) and six texture parameters were determined using the sessile drop and tangent line methods, as well as the sand patch and laser texture scanner techniques. To evaluate the ice–concrete adhesion, shear strength measurements obtained through interlayer shear instrument testing were utilized. In our analysis, we examined the relationship between ice adhesion strength and several factors, including the freezing temperature (T), water wettability, and surface texture parameters. A partial least squares (PLS) model was built to comprehensively analyze the effects of different factors on ice-concrete adhesion. The results indicate that improving hydrophobicity, as demonstrated by an increase in WCA from 20.4° to 119.4°, and raising the freezing temperature were both effective approaches for significantly reducing ice-concrete adhesion. The effects of different texture parameters on hydrophilic and hydrophobic concrete were significantly different. Specifically, for ordinary concrete, the ratio of the surface area (Sr) and the mean texture depth (MTD) demonstrated a positive correlation with ice adhesion strength. For hydrophobic surfaces, the MTD exhibited the greatest correlation with adhesion, followed by Sr. However, skewness (Rsk) also had a significant effect on the ice adhesion of hydrophobic concrete, and ice adhesion preferred valley-texture concrete. Finally, the PLS model results showed that the order of influence on ice-concrete adhesion was: Sr > WCA > MTD > T > Rsk. Based on our findings, we suggest three approaches for reducing ice adhesion to concrete surfaces: implementing semicircular or trapezoidal groove textures, reducing the surface energy of the concrete, and introducing the valley texture surfaces. This study focuses on the influence of surface characteristics of concrete pavements on ice adhesion and provides guidance on designing concrete surfaces for effective road de-icing.

Stabilization of AlH3 Crystals by the Coating of Hydrophobic PFPE and Resulted Reactivity with Ammonium Perchlorate.

Aluminum hydride (AlH3) is a promising fuel component of solid propellant, but its stabilization is still challenging. Herein, surface functionalization of hydrophobic perfluoropolyether (PFPE) followed by ammonium perchlorate (AP) coating has been implemented. In particular, AlH3@PFPE@xAP (x = 10, 30, 50, or 64.21%) composites (AHFPs) were prepared by a spray-drying technique. The PFPE-functionalized AlH3 with a hydrophobic surface shows an increased water contact angle (WCA) from 51.87° to 113.54°. Compared with pure AlH3, the initial decomposition temperatures of AHFPs were increased by 17 °C, and the decomposition properties of AP in the AHFPs were also enhanced with significantly decreased peak temperature and fairly increased energy output. Moreover, the decomposition induction time of AHFPs-30% was improved by almost 1.82 times that of raw AlH3, which indicates that the coatings of PFPE and AP could improve the stability of AlH3. The maximum flame radiation intensity of AHFPs-30% was 21.6 × 103, which is almost 7.71 times that of pure AlH3 (2.8 × 103).

X-aggregation-induced emission in newly fabricated Pullulan/3-Hydroxyflavone derivative composite electrospun nanofiber mat for optical applications

A fascinating optically important 3-Hydroxyflavone derivative 2-(2,5-dimethoxyphenyl)-3‑hydroxy-4H-chromen-4-one was synthesized and its single-crystal structure was studied. This compound was used as a dopant and incorporated into the pullulan matrix by electrospinning technique. Functionalized pullulan nanofiber mat was found to possess dopant molecules organized in an X-aggregated fashion accounting for the twisted structure of the dopant molecules. The diameter of the nanofiber mat was reduced from 250 nm to 120 nm upon fabrication with dopant due to the nanofiber mat's increased crystallinity. Dopant molecules imparted absorption and emission properties into the fabricated nanofiber mat and turned it to be highly fluorescent triggering yellowish-green emission with a large Stokes shift of 193 nm due to X-aggregation. The improved water resistance of the fabricated pullulan nanofiber mat was witnessed by an increased water contact angle from 27.3° to 62.5° due to the incorporation of hydrophobic dopant molecules. The thermal and mechanical stability of the fabricated nanofiber mat was improved upon fabrication. The predicted absolute quantum yield was obtained in the 34.1- 40.3% range. The optimum indirect optical band gap of 2.25–2.50 eV and refractive index of 2.1–3.4 for the designed nanofiber mat suggested the potential application as OLED material.

Spreading Behavior of Oil on Hierarchical Microstructured PET Surfaces Fabricated Using Hot‐Embossing Combined with Laser‐Based Methods

AbstractIn this study, the wetting behavior of microstructured polyethylene terephthalate (PET) foils for polar and nonpolar liquids produced by plate‐to‐plate hot embossing is investigated. For the embossing step, stainless steel plates are used as stamps, which are microstructured with single‐scaled and hierarchical textures using direct laser writing and two‐beam direct laser interference patterning. The imprinted microstructures, containing pillar‐ and line‐like textures, show increased water contact angles combined with a superoleophilic behavior. Time‐resolved measurements reveal that oil droplets spread rapidly on the hierarchical textures with velocities of up to 1.4 mm2 s−1. This functionalization of PET foils creates new opportunities for a wide range of industrial applications, such as the use of oil‐based instead of solvent‐based paints, an improved distribution of lubricants in mechanical components or for oil–water separation in maritime surroundings.