Search Results (273)

In winter, some roads face the problems of severe rain accumulation and ice formation, which pose major risks to traffic safety and result in substantial economic losses. With the development of hydrophobic materials, hydrophobic coatings have gradually gained attention as a novel anti-icing technology. In this study, utilizing vinyl triethoxysilane (VTES) as the monomer and benzoyl peroxide (BPO) as the initiator, a hydrophobic anti-icing coating for highway pavements was prepared through the free radical polymerization method. Through designing the icing rate test and ice–pavement interface adhesion strength test, combining the contact angle test technology, wet wheel abrasion test, and pendulum friction coefficient test, the anti-icing performance, durability, and skid resistance performance of the hydrophobic anti-icing coating under the three types of mixtures of asphalt concrete (AC-13), Portland cement concrete (PCC), and porous asphalt concrete (PAC-13) were evaluated. The results indicate that when the surface layer of the pavement was sprayed with anti-icing coating, the water was dispersed in a semi-spherical shape and easily rolled off the road surface. Compared to uncoated substrates, the anti-icing coating reduced the icing rate on the surface by approximately 25%. Comparing with the uncoated pavements mixtures, for AC-13, PCC, and PAC-13 pavements, the ice–pavement interface adhesion strength after the application of hydrophobic anti-icing coating reduced by 30%, 79% and 34%, respectively. Both cement pavements and asphalt pavements, after the application of hydrophobic anti-icing coating, expressed hydrophobic properties (contact angle of 131.3° and 107.6°, respectively). After wet wheel abrasion tests, the skid resistance performance of pavement surfaces coated with the hydrophobic anti-icing coating met the specification requirements. This study has great significance for the promotion and application of hydrophobic anti-icing technology on highway pavements. Full article

A series of porous carbons (PPC) derived from pomegranate peel were synthesized as catalyst supports for Pd/PPC catalysts via hydrothermal-carbonization and incipient wetness impregnation in an acetylene hydrochlorination reaction. The optimal Pd/PPC (500) catalyst with more than 99% of acetylene conversion and vinyl chloride monomer (VCM) selectivity was obtained using an orthogonal experimental design (OED) and single-factor experiments. Based on the catalytic performance and characterization of the Pd/PPC catalyst, the deactivation mechanism of the catalysts, which was attributed to carbon deposition on the catalysts’ surface, and the loss of active Pd species have been studied, which provides insights for the rational design of high-performance biomass-based acetylene hydrochlorination catalysts. Full article

A polyacrylamide-based film-forming agent was synthesized via free-radical copolymerization. FT-IR spectroscopy confirmed complete monomer conversion with no detectable residual unsaturation. Systematic variation of acrylamide (AM), vinyl acetate (VAc) and cellulose content revealed that an AM mass fraction of 3.7 wt%, a VAc:AM molar ratio of 1:3 and a cellulose content of 1.6 wt% yielded an emulsion of maximal colloidal stability. Under these conditions, the agent formed coherent, moisture-resistant films that effectively encapsulated sodium-bentonite pellets, indicating its potential as an efficient inhibitor for maintaining well-bore stability during drilling operations. Full article

A chemical platform for post-polymerization methods was developed, starting from the ecodesign and enzymatic synthesis of safe and sustainable bio-based polyesters containing discrete units of itaconic acid. This unsaturated bio-based monomer enables the covalent linkage of molecules that can impart desired properties such as hydrophilicity, flexibility, permeability, or affinity for biological targets. Molecular descriptor-based computational methods, which are generally used for modeling the pharmacokinetic properties of drugs (ADME), were employed to predict in silico the hydrophobicity (LogP), permeability, and flexibility of virtual terpolymers composed of different polyols (1,4-butanediol, glycerol, 1,3-propanediol, and 1,2-ethanediol) with adipic acid and itaconic acid. Itaconic acid, with its reactive vinyl group, acts as a chemical platform for various post-polymerization functionalizations. Poly(glycerol adipate itaconate) was selected because of its higher hydrophilicity and synthetized via solvent-free enzymatic polycondensation at 50 °C to prevent the isomerization or crosslinking of itaconic acid. The ecotoxicity and marine biodegradability of the resulting oligoester were assessed experimentally in order to verify its compliance with safety and sustainability criteria. Finally, the viability of the covalent linkage of biomolecules via Michael addition to the vinyl pendant of the oligoesters was verified using four molecules bearing thiol and amine nucleophilic groups: N-acetylcysteine, N-Ac-Phe-ε-Lys-OtBu, Lys-Lys-Lys, and glucosamine. Full article

Polyvinyl chloride (PVC) is the third most widely produced plastic on an industrial scale, due to its diverse applications and physicochemical properties. Its production through suspension polymerization presents significant safety challenges due to the handling of hazardous substances. To assess the impact of energy integration on process risks, the inherent safety analysis was implemented to determine the characteristic hazards of PVC suspension production. The methodology’s indicators were quantified by reviewing databases, literature, and safety data sheets, considering process steps such as vinyl chloride monomer recovery, PVC purification, and drying. The results revealed that the PVC production process under energy integration conditions is intrinsically unsafe, with a total inherent safety index (ISI) of 34. The chemical component would contribute 19 points, with VCM being the main chemical risk given its flammable and carcinogenic nature, contributing a value of 15, along with the heat released by the reactions. Process safety would contribute 15 points, associated with hazardous equipment such as furnaces, burners, and dryers, as well as risks related to inventories and similar plant accidents. To improve process safety, it is recommended to reduce VCM inventories, optimize operating conditions, and implement advanced control systems for possible accidental releases. Full article

Photopolymer PQ/PMMA, as a pivotal material in the field of holographic storage, demonstrates significant application potential owing to its advantages, such as straightforward preparation processes, cost-effectiveness, and tunable thickness. However, its practical application is still constrained by the need for further enhancement in key performance indicators, including diffraction efficiency, photosensitivity, and anti-aging properties. In this study, N-vinylpyrrolidone (NVP) is employed as a comonomer. By precisely controlling the doping ratio, we systematically investigate the influence mechanism of different NVP doping concentrations on the holographic performance of NVP-PQ/PMMA materials. Research indicates that the introduction of NVP effectively increases the vinyl concentration in the PQ/PMMA matrix, thereby directly generating photoproducts with PQ during the photoreaction process and further enhancing the photopolymerization process. Consequently, the holographic performance of the novel NVP-PQ/PMMA material is improved in a multi-faceted manner compared to ordinary PQ/PMMA. Specifically, the diffraction efficiency is enhanced by 1.93 times, the photosensitivity is increased by 1.64 times, the material uniformity is improved by 38%, and the light-induced shrinkage rate is reduced by 39%. Additionally, NVP-PQ/PMMA materials exhibit excellent stability and aging resistance in high-temperature accelerated aging experiments. Doping with a monomer of specific structure enhances the optical properties, providing broad adaptability for further research on PQ/PMMA photopolymer materials. Full article

Hydrogel materials have become an efficient, bioactive, and multifunctional alternative with great potential for biomedical applications. In this work, photoactive films were successfully designed for optical processing, and their photoactivity was tested in photodynamic therapy (PDT), such as antimicrobial patches. The stimulus-response hydrogel films are made of a hydrophilic polymer based on vinyl monomers, specifically 2-hydroxyethyl methacrylate (HEMA) and acrylamide (AAm), in a 1:1 molar ratio, along with the photochromic agent, 3,3-dimethylindolin-6′-nitrobenzoespiropirano (BSP), and a crosslinking agent, N,N’-methylenebisacrylamide (MBA). These hydrogel films were successfully created using the photoinitiator 2-hydroxy-4′-(2-hydroxyethoxy)-2-methylpropiophenone (IRGACURE 2959), MBA, and BSP in different concentrations (0.1, 0.3, and 0.5 mol%), which were later tested in photodynamic therapy (PDT) with the photosensitizer Ru(bpy)₂²⁺ against Staphylococcus aureus. The results showed that, while free Ru(bpy)₂²⁺ needed concentrations of 4–8 µg/mL to eliminate methicillin-sensitive (MSSA) strains, only partial inactivation was achieved for methicillin-resistant (MRSA) strains. The addition of the hydrogel films with BSP improved their effectiveness, lowering the minimum inhibitory concentration (MIC) to 2 µg/mL to fully inactivate MSSA and MRSA strains. These findings demonstrate that the combined use of hydrogel films containing BSP and Ru(bpy)₂²⁺ within a hydrogel matrix not only boosts antimicrobial activity but also highlights the potential of these photoactive films as innovative photosensitive antimicrobial coatings. This synergistic effect of BSP and Ru(bpy)₂²⁺ indicates that these materials are promising candidates for next-generation antimicrobial coatings and creative photosensitive materials. Full article

Polyvinyl chloride (PVC) remains one of the most widely used synthetic polymers worldwide, primarily due to its versatility, cost-effectiveness, and broad applicability across construction, healthcare, automotive, and consumer goods industries. However, its production involves hazardous chemicals, particularly vinyl chloride monomer (VCM), which requires rigorous safety assessments. In this context, the present study applies the Inherent Safety Index (ISI) methodology to evaluate the safety performance of a suspension polymerization process for PVC production that incorporates direct water recycling as a sustainability measure. The integration of water reuse reduces the fractional water consumption index from 2.8 to 2.2 and achieves a recovered water purity of 99.6%, demonstrating clear environmental benefits in terms of resource conservation. Beyond water savings, the core objective is to assess how this integration influences the inherent risks associated with the process. The key operational stages—polymerization, VCM recovery, product purification, and water recirculation—were modeled and analyzed using computer-aided process engineering (CAPE) tools. The ISI analysis yielded a score of 33, surpassing the threshold typically associated with inherently safer designs, with VCM hazards alone contributing a score of 19 due to its high flammability and carcinogenicity. These findings reveal a critical trade-off between environmental performance and inherent safety, underscoring that resource integration measures, while beneficial for sustainability, may require complementary safety improvements. This study highlights the necessity of incorporating inherently safer design principles alongside process integration strategies to achieve balanced progress in operational efficiency, environmental responsibility, and risk minimization in PVC manufacturing. Full article

Poly(N-vinyl-2-pyrrolidone), or PVP, nanogels loaded with gadolinium nitrate (Gd(NO₃)₃·6H₂O) were synthesized by ionizing irradiation, aiming for potential applications in magnetic resonance imaging (MRI). A comprehensive characterization of PVP and Gd aqueous solutions with different VP-monomer-to-Gd ratios was conducted before and after irradiation. The results indicate a complexation between PVP and Gd ions before irradiation. The size of the nanogels exhibited a strong dependence on several factors, including PVP molecular weight, concentration, temperature, and the precise timing of Gd introduction relative to the irradiation process. A quantification study was conducted to investigate the impact of molecular weight, the VP/Gd ratio, and Gd addition before or after the irradiation process on the concentration of free Gd ions. These findings offer valuable insights into optimizing the synthesis of Gd-loaded PVP nanogels for potential applications, highlighting the critical factors that influence their size and stability. Full article

The interest in macromolecular alkoxysilyl-functionalized hybrids (self-assembling or nanostructured), which could be used as precursors in biomimetic silica precipitation and for the synthesis of hollow spherical silica particles, is growing. Nevertheless, reports on all-organosilicon systems for bioinspired silica precipitation are scarce. Therefore, a new kind of polyalkoxysilane macromonomer–linear polysilsesquioxane (LPSQ) of ladder-like backbone, functionalized in side chains with trimethoxysilyl groups (LPSQ-R-Si(OMe)₃), was designed following this approach. It was obtained by photoinitiated thiol-ene addition of 3-mercaptopropyltrimethoxysilane to the vinyl-functionalized polysilsesquioxane precursor, carried out in situ in tetraethoxysilane (TEOS). The mixture of LPSQ-R-Si(OMe)₃ and TEOS (co-monomers) was used in a sol–gel process conducted under acidic conditions (0.5 M HCl/NaCl) in the presence of Pluronic^® F-127 triblock copolymer as a template. LPSQ-R-Si(OMe)₃ played a key role for the formation of microparticles of a spherical shape that were formed under the applied conditions, while their size (as low as 3–4 µm) was controlled by the stirring rate. The hybrid materials were hydrophobic and showed good thermal and oxidative stability. Introduction of zinc acetate (Zn(OAc)₂) as an additive in the sol–gel process influenced the pH of the reaction medium, which resulted in structural reinforcement of the hybrid microparticles owing to more effective condensation of silanol groups and a relative increase of the content of SiO₂. The proposed method shows directions in designing the properties of hybrid materials and can be translated to other silicon–organic polymers and oligomers that could be used to produce hollow silica particles. The established role of various factors (macromonomer structure, pH, and stirring rate) allows for the modulation of particle morphology. Full article

Bisphenol S (BPS), a key ingredient in polycarbonate plastics and epoxy resins, is a known endocrine-disrupting compound that poses significant risks to human health and the environment. As such, the development of rapid and reliable analytical techniques for its detection is essential. In this work, we present a newly engineered electrochemical sensor designed for the sensitive and selective detection of BPS using a straightforward and effective fabrication approach. The sensor was constructed by grafting molecularly imprinted polymers (MIPs) onto vinyl-functionalized multiwalled carbon nanotubes (f-MWCNTs). Ethylene glycol dimethacrylate and acrylamide were used as the cross-linker and functional monomer, respectively, in the synthesis of the MIP layer. The resulting MIP@f-MWCNT nanocomposite was characterized using Fourier-transform infrared spectroscopy (FT-IR) and scanning electron microscopy (SEM). The MIP@f-MWCNT material was then combined with chitosan, a biocompatible binder, to fabricate the final MIP@f-MWCNT/chitosan-modified glassy carbon electrode (GCE). Electrochemical evaluation showed a broad linear detection range from 1 to 60 µM (R² = 0.992), with a sensitivity of 0.108 µA/µM and a detection limit of 2.00 µM. The sensor retained 96.0% of its response after four weeks and exhibited high selectivity against structural analogues. In spiked plastic extract samples, recoveries ranged from 95.6% to 105.0%. This robust, cost-effective, and scalable sensing platform holds strong potential for environmental monitoring, food safety applications, and real-time electrochemical detection of endocrine-disrupting compounds like BPS. Full article

Protein phosphorylation is one of the most common and important post-translational modifications (PTMs) and is highly involved in various biological processes. Ideal adsorbents with high sensitivity and specificity toward phosphopeptides with large coverage are therefore essential for enrichment and mass spectroscopy-based phosphoproteomics analysis. In this study, a newly designed IMAC adsorbent composite was constructed on the graphene matrix coated with mesoporous silica. The outer functional 3D-network layer was prepared by free radical polymerization of the phosphonate-functionalized vinyl imidazolium salt monomer and subsequent metal immobilization. Due to its unique structural feature and high content of Ti⁴⁺ ions, the resulting phosphonate-immobilized adsorbent composite G@mSiO₂@PPFIL-Ti⁴⁺ exhibits excellent performance in phosphopeptide enrichment with a low detection limit (0.1 fmol, tryptic β-casein digest) and superior selectivity (molar ratio of 1:15,000, digest mixture of β-casein and bovine serum albumin). G@mSiO₂@PPFIL-Ti⁴⁺ displays high tolerance to loading and elution conditions and thus can be reused without a marked decrease in enrichment efficacy. The captured phosphopeptides can be released globally, and mono-/multi-phosphopeptides can be isolated stepwise by gradient elution. When applying this material to enrich phosphopeptides from human lung cell lysates, a total of 3268 unique phosphopeptides were identified, corresponding to 1293 phosphoproteins. Furthermore, 2698 phosphorylated peptides were found to be differentially expressed (p < 0.05) between human lung adenocarcinoma cells (SPC-A1) and human normal epithelial cells (Beas-2B), of which 1592 were upregulated and 1106 were downregulated in the cancer group. These results demonstrate the material’s superior enrichment efficiency in complex biological samples. Full article

Water regeneration in PVC production is a key issue to consider, given the high freshwater consumption rate of the process. This research evaluates the inherent safety of poly(vinyl chloride) (PVC) production via suspension polymerization by implementing mass and energy integration strategies in combination with wastewater regeneration under a zero-liquid-discharge (ZLD) approach. The impact of these integrations on process safety was examined by considering the risks associated with the handling of hazardous materials and critical operations, as well as the reduction in waste generation. To this end, the Inherent Safety Index (ISI) methodology was employed, which quantifies hazards based on factors such as toxicity and flammability, enabling the identification of risks arising from system condition changes due to the implementation of sustainable water treatment technologies. Although the ISI methodology has been applied to various chemical processes, there are few documented cases of its specific application in PVC plants that adopt circular production strategies and water resource sustainability. Therefore, in this study, ISI was used to thoroughly evaluate each stage of the process, providing a comprehensive picture of the safety risks associated with the use of sustainable technologies. The assessment was carried out using simulation software, computer-aided process engineering (CAPE) methodologies, and information obtained from safety repositories and expert publications. Specifically, the Chemical Safety Index score was 22 points, with the highest risk associated with flammability, which scored 4 points, followed by toxicity (5 points), explosiveness (2 points), and chemical interactions, with 4 points attributed to vinyl chloride monomer (VCM). In the toxicity sub-index, both VCM and PVC received 5 points, while substances such as sodium hydroxide (NaOH) and sodium chloride (NaCl) scored 4 points. In the heat of reaction sub-index, the main reaction scored 3 points due to its high heat of reaction (−1600 kJ/kg), while the secondary reactions from PVA biodegradation scored 0 points for the anoxic reaction (−156.5 kJ/kg) and 3 points for the aerobic reaction (−2304 kJ/kg), significantly increasing the total index. The Process Safety Index scored 15 points, with the highest risk found in the inventory of hazardous substances within the inside battery limits (ISBL) of the plant, where a flow rate of 3241.75 t/h was reported (5 points). The safe equipment sub-index received 4 points due to the presence of boilers, burners, compressors, and reactors. The process structure scored 3 points, temperature 2, and pressure 1, reflecting the criticality of certain operating conditions. Despite sustainability improvements, the process still presented significant chemical and operational risks. However, the implementation of control strategies and safety measures could optimize the process, balancing sustainability and safety without compromising system viability. Full article

Porous materials are used in many important applications, such as separation technologies, catalysis, and chromatography. They may be obtained from various monomers via diverse polymerization techniques and a wide range of synthesis parameters. The study is devoted to the synthesis and characterization of crosslinked porous polymeric spheres containing pyrrolidone subunits. To achieve this goal, two methods were applied: direct synthesis from N-vinyl-2-pyrrolidone (NVP) with ethylene glycol dimethacrylate (EGDMA) and via a modification reaction of porous poly(glycidyl methacrylate-co-ethylene glycol dimethacrylate) with pyrrolidone (P). The polymerization was carried out with the use of different molar ratios of the monomers. In order to obtain highly porous materials, pore-forming diluents (toluene, dodecane, and dodecan-1-ol) were used. The synthesized copolymers were characterized using size distribution analysis, ATR-FTIR spectroscopy, scanning electron microscopy, thermogravimetry, and inverse gas chromatography. Determined by the nitrogen adsorption/desorption method, the specific surface area was in the range of 55–468 m²/g. The good thermal properties of the poly(VP-co-EGDMA) copolymers allowed them to be applied as the stationary phase in gas chromatography. Full article

Cured-in-place pipe (CIPP) technology is a trenchless rehabilitation method for damaged pipelines in which a resin-saturated liner (often a fiber-reinforced type) is inserted into a host pipe and cured in situ, typically using a UV light beam or steam. This study investigates the influence of selected photoreactive diluents on the photopolymerization process of a styrene-free vinyl ester resin designed for the CIPP applications by evaluating the rheological properties, photopolymerization kinetics (photo-DSC), thermal characteristics (DSC), crosslinking density (gel content), and mechanical properties of thick (15 mm) UV-cured layers. The tested diluents included monofunctional (i.e., methyl methacrylate and vinyl neodecanoate), difunctional (1,6-hexanediol diacrylate, aliphatic urethane acrylates, and an epoxy acrylate), and trifunctional monomers (trimethylolpropane triacrylate, pentaerythritol triacrylate, and trimethylolpropane ethoxylate triacrylate). The key findings demonstrate that the addition of pentaerythritol triacrylate (the most attractive diluent) increases the flexural strength (+6%) and deflection at strength (+28%) at the unchanged flexural modulus value (ca. 2.1 GPa). The difunctional epoxy acrylate caused an even greater increase in the deflection (+52%, at a 5% increase in the flexural strength). Full article