Search Results (402)

Alkyd resins are among the most common coatings used for exterior wood joinery. In Romania, solvent-borne alkyd coatings are widely used to finish wood. The study aims to compare the performance after 7 years of outdoor exposure of two types of alkyd coatings, a semi-transparent brown stain with micronized pigments (Alk1) and an opaque white enamel (Alk2), applied directly on wood or wood pre-treated with three types of resins: acryl-polyurethane (R1), epoxy (R2), and alkyd-polyurethane (R3). Fir (Abies alba) wood served as the substrate. Cracking, coating adhesion, and biological degradation were periodically assessed through visual inspection and microscopy. Additionally, a cross-cut test was performed, and the loss of coating on the directly exposed upper faces was measured using ImageJ. The results indicated that resin pretreatments somewhat reduced cracking but negatively affected coating adhesion after long-term exposure. All samples pretreated with resins and coated with Alk1 lost more than 50% (up to 78%) of the original finishing film by the end of the test. In comparison, coated control samples lost less than 50%. The Alk2 coating exhibited a film loss between 2% and 12%, compared to an average loss of 9% for the coated control. Overall, samples pretreated with alkyd-polyurethane resin (R3) and coated with alkyd enamel (Alk2) demonstrated the best performance in terms of cracking, adhesion, and discoloration. Full article

Chiral molecules are crucial in the field of optical devices, molecular recognition, and other novel functional materials due to their unique spatially asymmetric configuration and optical activity. In this study, a chiral molecule, Cholest-3-yl (E)-3-(4-carbamoylphenyl)acrylate (CCA), was combined with dyes containing large conjugated structures, tetramethylporphyrin tetrasulfonic acid (TPPS), and Nickel(II) phthalocyanine-tetrasulfonic acid tetrasodium salt (TsNiPc), and composite LB films of CCA/TPPS and CCA/TsNiPc were successfully prepared by using Langmuir-Blodgett (LB) technology. The circular dichroism (CD) test proved that the CCA/TPPS composite film had a strong CD signal at 300–400 nm, and the composite film showed chirality. This significant optical activity provides a new idea and option for the application of LB films in chiral sensors. In the Surface Enhanced Raman Spectroscopy (SERS) test, the CCA/TPPS composite film was sensitive to signal sensing, in which the enhancement factor EF = 2.28 × 10⁵, indicating that a large number of effective signal response regions were formed on the surface of the film, and the relative standard deviation (RSD) = 12.08%, which demonstrated that the film had excellent uniformity and reproducibility. The high sensitivity and low signal fluctuation make the CCA/TPPS composite LB film a promising SERS substrate material. Full article

Background and Objectives: Posterior chamber phakic implantable contact lenses (Phakic-ICL) are widely used for refractive correction due to their efficacy and safety, including minimal corneal endothelial cell loss. The Collamer-based EVO+ Visian implantable contact lens (ICL), manufactured from Collamer, which is a blend of collagen and hydroxyethyl methacrylate (HEMA), has demonstrated excellent long-term biocompatibility and optical clarity. Recently, hydrophilic acrylic Phakic-ICLs, such as the Implantable Phakic Contact Lens (IPCL), have been introduced. This study investigated the material differences among Phakic-ICLs and their interaction with fibronectin (FN), which has been reported to adhere to intraocular lens (IOL) surfaces following implantation. The aim was to compare Collamer, IPCL, and LENTIS lenses (used as control) in terms of FN distribution and cell adhesion using a small number of explanted Phakic-ICLs. Materials and Methods: Three lens types were analyzed: a Collamer Phakic-ICL (EVO+ Visian ICL), a hydrophilic acrylic IPCL, and a hydrophilic acrylic phakic-IOL (LENTIS). FN distribution and cell adhesion were evaluated across different regions of each lens. An in vitro FN-coating experiment was conducted to assess its effect on cell adhesion. Results: All lenses demonstrated minimal FN deposition and cellular adhesion in the central optical zone. A thin FN film was observed on the haptics of Collamer lenses, while FN adhesion was weaker or absent on IPCL and LENTIS surfaces. Following FN coating, Collamer lenses supported more uniform FN film formation; however, this did not significantly enhance cell adhesion. Conclusions: Collamer, which contains collagen, promotes FN film formation. Although FN film formation was enhanced, the low cell-adhesive properties of HEMA resulted in minimal cell adhesion even with FN presence. This characteristic may contribute to the long-term transparency and biocompatibility observed clinically. In contrast, hydrophilic acrylic materials used in IPCL and LENTIS demonstrated limited FN interaction. These material differences may influence extracellular matrix protein deposition and biocompatibility in clinical settings, warranting further investigation. Full article

This study focuses first on the synthesis through an aza-Michael addition reaction of original linear diamine prepolymers and original amine/acrylate thermoset adhesives, and second on their thermal, mechanical and adhesion characterization. The major advantage of the aza-Michael addition reaction is that it takes place at room temperature, without a solvent and without a catalyst. Using the aza-Michael addition reaction, linear secondary diamine prepolymers were first synthesized with a control of the molecular weight, ranging from 867 to 1882 g mol⁻¹. Then, aza-Michael reactions of diamine prepolymers with three different acrylates allowed the synthesis of new amine/acrylate thermoset adhesives. All the thermoset adhesives were characterized by rheology and thermal analysis, leading, once the crosslinking aza-Michael reaction had occurred, to soft thermoset networks with glass transition temperatures ranging from −23 to −8 °C, gel point times ranging from 40 min to 4 h, and a polar component of the surface energy ranging from 3 to 17 mJ m⁻². Functionality of the acrylates directly influences the crosslinking rate, and a decreasing master curve is obtained when reporting crosslinking rate versus gel point time. Crosslinking density is controlled by the diamine prepolymer chain length. In a second step, thermoset adhesives were applied as thin films between two galvanized steel plates, and adhesion properties were evaluated through a lap-shear test. Results showed that the adhesive strength increases as the dynamic viscosity and molecular weight of the diamines prepolymer increases. Increasing the diamines prepolymer chain length results in an increase in strain at break, a decrease in the shear modulus, and a decrease in the maximum lap-shear strength. It is also observed that the adhesive strength decreases when the adhesive film thickness increases. Moreover, thermoset adhesives with high polarity and a surface energy similar to the surface energy of the substrate will favor high adhesion and a better adhesive strength of the assembly. Lastly, the nature of the acrylates and diamines prepolymer chain length allow tuning a wide range of adhesive strength and toughness of these original soft thermoset adhesives. Full article

Winter pavement maintenance faces challenges in balancing large-scale upkeep and driving safety, particularly regarding the application of active slow-release materials. This study proposes a gel-modified salt-storing ceramsite asphalt mixture to enhance ice-melting capabilities through controlled salt release. By replacing a conventional coarse aggregate with salt-storing ceramsite in SMA-10 graded mixtures (0–80% content), we systematically evaluate its mechanical performance and de-icing functionality. The experimental results demonstrate that 40% salt-storing ceramsite content optimizes high-temperature stability while maintaining acceptable low-temperature performance and water resistance. Microstructural analysis reveals that silicone–acrylic emulsion forms a hydrophobic film on ceramsite surfaces, enabling uniform salt distribution and sustained release. The optimal 10% gel modification achieves effective salt retention and controlled release through pore-structure regulation. These findings establish a 40–60% salt-storing ceramsite content range as the practical range for winter pavement applications, offering insights into the design of durable snow-melting asphalt surfaces. Full article

Cholesteric liquid crystal polymer network (CLCN) films with composite structural colors have potential applications in decoration and anti-counterfeiting. Herein, a thermochromic acrylate-based cholesteric liquid crystal mixture was prepared. The structural color of CLCN films can be controlled by the photopolymerization temperature. Based on the oxygen inhibition of the acrylate group, CLCN films with double reflection bands were prepared using a two-step photopolymerization method. The distance between these two reflection bands was controlled by the polymerization temperatures of these two steps. Since golden colors are the most attractive for decoration, herein, colorful patterns with a golden structural color were prepared by controlling the polymerization temperatures. Full article

Currently, for the treatment of corneal diseases (keratitis–corneal opacities), synthetic corneal analogs based on polymer films or hydrogels are being developed. The requirements for the material include biocompatibility, the presence of a developed system of macropores, transparency, rapid swelling, and mechanical strength. Here, with the aim of preparing such materials, a series of gels based on a copolymer of 2-acrylamido-2-methyl-1-propanesulfonic acid (AMP) and 2-hydroxyethyl methacrylate (or vinyl acetate, or ethyl acrylate) were obtained using cryotropic gelation. It was shown that transparent cryogels can be obtained based on the sulfonate-containing comonomer 2-acrylamido-2-methyl-1-propanesulfonic acid at a crosslinking agent concentration of 2.2 mol.%, while the nature of the acrylate comonomer did not show any effect on transparency. It was found that when using AMP and ethyl acrylate, cryogels with a developed system of macropores with a diameter of 50 to 250 μm were formed, and the mechanical strength of such cryogels was sufficient for their subsequent use as corneal implants. Moreover, the PAMP hydrogel containing 2-hydroxyethyl methacrylate or ethyl acrylate units did not affect the viability of cells even after 1 month. Full article

This study investigated the influence of different functional groups on the electro-optical properties of polymer-dispersed liquid crystal (PDLC) films. Twelve acrylate monomers with functional groups like amino, halogen, and double-bond were introduced into PDLC films, and twelve samples were prepared. The electro-optical properties and microstructure of the films were characterized. The results show that compared to films with amino and halogen groups, those with hydroxyl groups have the best balance of driving voltage and contrast, achieving higher contrast at lower driving voltage, making this preparation scheme ideal for low-voltage, high-contrast PDLC films. Also, in the presence of hydroxyl groups, introducing double bonds increases saturation voltage and decreases saturation. Hydrogen-bond engineering through strategically positioned hydroxyl groups in acrylate monomers optimizes PDLC performance by enabling compact polymer networks and controlled phase separation, achieving superior contrast ratios (163) and low saturation voltages (15.8 V), while amino groups induce steric limitations and dual-bond systems that disrupt hydrogen-bond efficacy, highlighting hydroxyl spatial design as critical for electro-optical optimization. Full article

Sealing treatment is widely used as a simple and low-cost process to improve the long-term corrosion resistance of Fe-based amorphous coatings. In this study, an eco-friendly graphene modified waterborne acrylic sealant(WFS) with strong permeability was prepared by emulsion polymerization and GO@SiO₂ was introduced as a reinforcing material to increase the withstand resistance of the hybrid sealant to Cl⁻. A combination of ultrasonic excitation and vacuum sealing effectively promotes the penetration of the waterborne hybrid sealant into the pores of the coating. A 3D X-ray scan confirmed the sealant penetration depth of 160 μm. The natural properties of the emulsion were characterized by a particle size analyzer, FTIR, TGA-DSC and TEM. Potentiodynamic polarization curves and AC impedance spectroscopy analysis showed that GO@SiO₂ has a strong blocking ability to Cl⁻, which greatly promotes the integrity of the passive film. It is anticipated that the novel eco-friendly waterborne hybrid sealants with strong permeability will find applications in a variety of porous hard coatings. Full article

This study examines the surface-dependent formation of interpolymer complexes (IPCs) by the layer-by-layer (LBL) deposition method. The materials used in this analysis are poly(acrylic acid) (PAA) combined with cellulose ethers, namely methyl cellulose (MC), hydroxypropyl cellulose (HPC), and hydroxyethyl cellulose (HEC), and poloxamers PX188 and PX407. PMMA, PS, and glass surfaces have been used to study the influence of hydrophobicity and hydrophilicity on IPC growth and its properties. Through contact angle measurements, PMMA and PS were found to be hydrophobic and glass hydrophilic. It was revealed by gravimetric analysis that IPC films reveal the highest growth on PMMA substrates, followed by PS and glass. Both the molecular weight of HEC and the hydrophobicity of the surface considerably affected the growth. Hydrogen-bonded complexation was evident by means of FTIR spectroscopy, while changes in some characteristic absorption bands demonstrated the extent of interactions between polymers. Scanning electron microscopy showed that variations in the microstructure of surfaces occur; PAA-MC and poloxamer complex layers were well organized on hydrophobic substrates. Thus, the experimental results showed surface properties, especially hydrophobicity, to be important for IPC growth and structure. These findings contribute to the understanding of IPC behavior on different substrates, thus giving insights into applications in drug delivery, coatings, and functional films. Full article

Money Art is a growing contemporary practice where artists transform banknotes into unique visual works. While conceptually powerful, these artworks present significant conservation challenges due to their fragile substrates and complex material compositions. This study investigates the degradation behaviour of UniPosca acrylic markers applied on zero-euro banknotes, drawing on the techniques of artist RichardHTT, and explores bio-based protective strategies suitable for their preservation. Laboratory samples were prepared to replicate the original artwork and subjected to accelerated ageing. A multi-analytical approach was employed, including multispectral imaging, Fourier trasform infrared (FTIR) and Raman spectroscopy, and scanning electron microscopy (SEM-EDS) colorimetric analysis. Thickness and adhesion properties were assessed with contact micrometry and peel tests, while wettability was evaluated through static contact angle measurements. Four biopolymer coatings, chitosan and chitosan–nanocellulose films with varying CNC concentrations, were evaluated for their transparency, mechanical stability, and compatibility with the substrate. Results showed that painted areas, especially those with blue and black pigments, experienced marked degradation, while, after coating application, samples demonstrated improved chromatic stability, hydrophobicity, and adhesion. Importantly, all coatings were fully removable via enzymatic cleaning with α-amylase, confirming their reversibility. This research highlights the potential of chitosan-based biocomposites as conservation materials for non-traditional artworks and contributes to developing tailored, reversible strategies for contemporary art preservation. Full article

This study uses the melt compounding method to recycle polypropylene-based car bumper waste (PP-CBW) in order to produce nanocomposite films for mulch application. The nanocomposite films were compounded by mixing virgin linear low-density polyethylene (LLDPE) with PP-CBW at a constant ratio of 4:1 in the presence of different percentages of nanofillers. Nanocomposites reinforced with nanoclays were compatibilized with an anhydride grafted polyethylene (PE-g-MAH), at a constant compatibilizer-to-clay ratio equal to 3, to improve the adherence between the nonpolar matrix and the hydrophilic nanoclay and acrylic paint present in the car bumper. An extruder with a corotating twin screw was used to produce blends of different compositions. To create nanocomposite films, the mixtures were further processed in a blown film extruder. The effect of the presence of nanoclays on the barrier, thermal, and mechanical properties of the nanocomposite films was investigated. The dispersion of clay layers in the matrix was examined by atomic force microscopy (AFM). The results indicate that 3 wt% of clay loading maximized the tensile strength in the transverse direction (TD) and machine direction (MD). A 1 wt% clay loading increased the MD tear resistance by 66% and manifested an optimum dart impact strength. Significant improvements in thermal and barrier properties were also achieved in the presence of 3 wt% clay loading. Full article

The photosensitive properties of smart photoactive polymers give them a wide range of potential applications across various fields. This study focuses on designing polymeric systems that incorporate hydrophilic polymers, with the primary goal of adapting these materials for biological applications. Specifically, it aims to contribute to the development of photochromic materials for optical processing, utilizing both molecular and macromolecular components. Additionally, this study evaluates the effectiveness of photoactive polymers in photodynamic therapy (PDT). It details the synthesis and characterization of photoactive copolymers derived from maleic anhydride (MAn) combined with vinyl monomers such as 2-methyl-2-butene (MB) and 1-octadecene (OD), as well as the organic compound 1-(2-hydroxyethyl)-3,3-dimethylindoline-6-nitrobenzopyran (SP). The two novel optically active alternating polymeric systems, poly(maleic anhydride-alt-octadecene) and poly(maleic anhydride-alt-2-methyl-2-butene), were functionalized with SP through an esterification process in a 1:1 monomer feed ratio, using pyridine as a catalyst. This methodology incorporated approximately 100% of the photoactive molecules into the main acrylic chain to prepare the alternating copolymers. These copolymers were characterized by UV-visible, FTIR, and 1H-NMR spectroscopy and analysis of their optical and thermal properties. When exposed to UV light, the photoactive polymer films can develop a deep blue color (566 nm in the absorption spectra). Finally, the study also assesses their capacity for photodynamic antimicrobial action in organic film. Notably, the photoactive P(MAn-alt-2MB)-PS significantly enhances the photodynamic antimicrobial activity of the photosensitizer Ru(bpy) against two bacterial strains of Staphylococcus aureus, reducing the minimum inhibitory concentration (MIC) from 2 µg/mL to 0.5 µg/mL. Therefore, 4 times less photosensitizer is required when mixed with the photoactive polymer to inhibit the growth of antibiotic-sensitive and -resistant bacteria. Full article

Background: Nail gels are decorative fingernail coatings based on (meth)acrylates that are photopolymerized on the nail surface. After polymerization, these coatings typically retain an uncured layer of monomers at the air interface due to oxygen inhibition, which may pose a risk of skin sensitization unless removed. No-wipe topcoats are formulated to address this issue by curing fully; however, no standard test method exists to verify a complete cure. This study presents a method to quantify residual uncured traces of several common nail gel monomers extracted from polymerized commercial no-wipe nail gels. Method: Commercially available no-wipe nail gels were formed into films of controlled thickness and polymerized using a standard UV-curing nail lamp. Solvent extraction was employed to eliminate residual uncured monomers, namely diethylene glycol dimethacrylate (DEGDMA), isobornyl acrylate (IBOA), and 2-hydroxyethyl methacrylate (HEMA). These monomers were quantified utilizing GC-FID and HPLC techniques. Method validation was conducted with samples of known monomer identity and concentration, thereby establishing specificity, linearity, precision, and detection limits. Results: Validated test protocols were established for the analysis of residual uncured traces of three commonly used monomers in nail gel coatings. In all instances, levels of monomer residue in a cured gel coating were found to range from 56 µg/g to 800 µg/g. Tests conducted on commercial products indicated that levels of these monomers fell within the expected normal ranges for such products. Conclusions: Through the utilization of two chromatographic techniques, three analytical methods were established for the simultaneous determination of ingredient concentrations and residual monomer quantities in unreacted bulk formula and cured UV-gel film. These methods and the resultant data facilitate the evaluation of curing completeness, which is essential for product development and safety assessments. Full article

As far as history tells, people have set efforts both to improve the conditions and to change the visual outfit of the skin, nails, and hair. The first information on nail cosmetics is found in ancient China and Egypt, where various nature-derived compositions were used for changing the colour of the nails. Nowadays more mechanically and chemically durable systems for nail polishes are elaborated. This review focuses on the latest achievements in the field of UV-curable nail polishes. Herein, the polymerization mechanisms of various systems (acrylates, as well as epoxides and thiols) occurring in nail polishes are described. Besides plausible side reactions of the polymerization process are characterized. Thus, the main drawbacks for forming a uniform, perfect layer are illuminated. For effective curing, the choice of photoinitiators may be crucial; thus, various types of photoinitiators as well as their main advantages and disadvantages are characterized. Ensuring effective adhesion between the substrate (human nail) and the polymer film is one of the challenges for the nail polish industry—thus the plausible interactions between the adhesion promoters and the keratin are described. Regarding the film-forming agents, a comprehensive overview of the composition of the traditional UV-curing nail polishes is provided, but the main emphasis is devoted to alternative, nature-derived film-forming agents that could introduce renewable resources into nail cosmetics. Additionally, this review gives short insight into the latest innovations in UV-curing nail cosmetics, like (1) nail polishes with improved pealability, (2) covalently polymer-bonded dyes and photoinitiators, thus reducing the release of the low-molecular compounds or their degradation products, and (3) UV-curing nail polishes as delivery systems for nail treatment medicine. Full article