Search Results (16)

The adsorptive removal of Bisphenol A (BPA) with the PE meshes photografted with 2-(dimethylamino)ethyl methacrylate (DMAEMA) was performed by varying the grafted amount, pH value, BPA concentration, and temperature, and the adsorption performance was correlated by the equilibrium, kinetic, and isotherm models. In addition, the regeneration of DMAEMA-grafted PE (PE-g-PDMAEMA) meshes was discussed from the repetitive adsorption/desorption process. The adsorption capacity had the maximum value at the grafted amount of 2.6 mmol/g and at the initial pH value of 8.0. The increase in the protonation of dimethylamino groups on grafted PDMAEMA chains and the dissociation of phenol groups of BPA present in the outer solution during the adsorption process results in the increase in BPA adsorption. The adsorption process followed the pseudo second-order equation. The BPA adsorption was enhanced by increasing the BPA concentration and the equilibrium data fit to Langmuir equation. The adsorption capacity stayed almost constant with the increase in the temperature, whereas the k₂ value increased against the temperature. These results comprehensively emphasized that BPA adsorption occurred through the chemical interaction or ionic bonding of a BPA anion to a terminal protonated dimethylamino group. Desorption of BPA increased by increasing the NaOH concentration and BPA was entirely desorbed at more than 20 mM. The cycle of adsorption at pH 8.0 and desorption in a NaOH solution at 100 mM was repeated five times without loss or structural damage. These results indicate PE-g-PDMAEMA meshes can be used as a regenerative adsorbent for BPA removal from aqueous medium. Full article

This study aims at the modification of the surface properties of twill-5 polyethylene terephthalate (PET) fabric, in particular to improve its hydrophilicity. It compares the hydrophilic potential and efficacy of two vinyl monomers radically grafted onto the fabric by photoinduced processes. Poly(ethylene glycol) diacrylate (PEGDA) and [2-(methacryloyloxy)-ethyl]-trimethylammonium chloride (METAC) affected the wettability of the fabric towards water, significantly reducing the water contact angle (WCA). As a consequence, the treated fabrics showed a good improvement of dynamic moisture management. Adopting specific conditions (e.g., type of monomer and grafting monomer concentration), the grafted PET fabrics remained hydrophilic after washing, laudering, dry cleaning, and rubbing tests; thus, the surface treatment modification resulted to be durable overall. Full article

Photo-grafting is a gentle, simple, and precise approach to incorporating specific functional molecules for the surface functionalization of substrates. In this work, ultraviolet (UV)-induced tannic acid (TA) grafting onto the surface of bamboo was proposed as a viable strategy for functionalizing bamboo. X-ray photoelectron spectroscopy (XPS) and Fourier transform infrared spectroscopy (FTIR) clearly indicated that TA was successfully introduced to the bamboo’s surface. The optimal conditions for the grafting reaction were determined to be 15 mM Methyl-2-benzoylbenzoate (BB), 30 mM TA, 20 min, and a pH = 8. Under these conditions, the amount of TA grafted onto the bamboo’s surface was measured to be 19.98 μg/cm². Results from Inductively Coupled Plasma (ICP) and Energy Dispersive Spectrometer (EDS) analyses showed that the silver ion loading capacity of tannic acid-grafted bamboo was significantly improved compared to that of raw bamboo and tannic acid-impregnated bamboo. Furthermore, the presence of TA grafted on the bamboo’s surface exhibited a positive correlation with the loading of silver ions, indicating that grafted TA plays an important role in the surface functionalization of bamboo. We believe that photo-grafted TA may help generate multifunctional bamboo with diverse properties. Full article

Vast amounts of dyeing wastewater released from the textile industry can not only cause water pollution but also have negative effects on the human body, such as skin irritation and respiratory diseases. Dye adsorption technology is necessary for the treatment of wastewater discharged from the dyeing industry and for environmental improvement. However, to remove dyeing wastewater, more energy and solvents are used to fabricate adsorbents, or excessive energy is used to filter dyeing wastewater out, resulting in more environmental pollution. Therefore, it is necessary to develop a method of filtering dyeing wastewater in a more environmentally friendly manner by minimizing the use of solvents and energy. In this study, we modified the surface of a textile substrate through UV irradiation to create a monomer capable of facilely bonding with dyes. Employing the UV photografting method, we were able to produce a dye adsorption filter in a more environmentally friendly manner, minimizing solvent usage and heat energy consumption required for absorbent synthesis. At a monomer concentration of 10%, the fabricated filter exhibited a dye removal efficiency of 97.34% after 24 h, all without the need for a pressure treatment or temperature increase. Moreover, it displayed an adsorption capacity of approximately 77.88 mg per 1 g of filter material. Full article

This study aims to confer autohesive strength to polyethylene (PE) plates by swelling the grafted layers, which were formed on the PE plates grafted with alkyl (meth)acrylate monomers, with 1,4-dioxane, and subsequently heat-pressing them. For the methyl methacrylate (MMA)-grafted PE (PE-g-PMMA) plates, the location of grafting was restricted to the outer surface region and the grafted layer with higher densities of grafted PMMA chains was composed. When the grafted PE plates were immersed in 1,4-dioxane, and then heat-pressed while applying the load, autohesion was developed. The substrate failure was observed for the PE-g-PMMA plates and the grafted amount at which the substrate failure was observed decreased with the procedures that decreased the methanol concentration of the solvent, the MMA concentration, the grafting temperature, and the heat-press temperature, and/or increased the load. The lowest grafted amount of 45 μmol/cm² for the substrate failure was obtained under the conditions where the PE-g-PMMA plate prepared at 0.75 M and 60 °C in a 70 vol% aqueous methanol solution was heat-pressed at 60 °C while applying the load of 2.0 kg/cm². The swelling of the grafted layers with 1,4-dioxane considerably contributed to the development of autohesion, bringing the inter-diffusion of grafted PMMA chains and coincident entanglement of grafted PMMA chains during the heat-pressing. The fact that the substrate failure occurred indicates that an autohesive strength higher than the ultimate strength of the used PE plate was obtained. Our approach provides a novel procedure to develop the water-resistant autohesion of PE plates. Full article

In this study, we developed highly efficient nonwoven membranes by modifying the surface of polypropylene (PP) and poly(butylene terephthalate) (PBT) through photo-grafting polymerization. The nonwoven membrane surfaces of PP and PBT were grafted with poly(ethylene glycol) diacrylate (PEGDA) in the presence of benzophenone (BP) and metal salt. We immobilized tertiary amine groups as BP synergists on commercial nonwoven membranes to improve PP and PBT surfaces. In situ Ag, Au, and Au/Ag nanoparticle formation enhances the nonwoven membrane surface. SEM, FTIR, and EDX were used to analyze the surface. We evaluated modified nonwoven membranes for photocatalytic activity by degrading methylene blue (MB) under LED and sunlight. Additionally, we also tested modified membranes for antibacterial activity against E. coli. The results indicated that the modified membranes exhibited superior efficiency in removing MB from water. The PBT showed the highest efficiency in dye removal, and bimetallic nanoparticles were more effective than monometallic. Modified membranes exposed to sunlight had higher efficiency than those exposed to LED light, with the PBT/Au/Ag membrane showing the highest dye removal at 97% within 90 min. The modified membranes showed reuse potential, with dye removal efficiency decreasing from 97% in the first cycle to 85% in the fifth cycle. Full article

A simple and compact intensity-interrogated terahertz (THz) relative humidity (RH) sensing platform is successfully demonstrated in experiments on the basis of combining a porous polymer sensing membrane and a continuous THz electronic system. The RH-sensing membrane is fabricated by surface modification of a porous polymer substrate with hydrophilic and photosensitive copolymer brushes via a UV-induced graft-polymerization process. The intensity interrogation sensing scheme indicated that the power reduction of the 0.4 THz wave is dependent on the grafting density of the copolymer brushes and proportional to the RH percent levels in the humidity-controlled air-sealed chamber. This finding was verified by the water contact angle measurement. Based on the slope of the proportional relation, the best sensitivity of the hydrophilic surface-modified sensing membrane was demonstrated at 0.0423 mV/% RH at the copolymer brush density of 1.57 mg/mm³ grafted on the single side of the sensing membrane. The sensitivity corresponds to a detection limit of approximately 1% RH. The THz RH sensing membrane was proven to exhibit the advantages of low loss, low cost, flexibility, high sensitivity, high RH resolution, and a wide RH working range of 25–99%. Thus, it is a good candidate for novel applications of wearable electronics, water- or moisture-related industrial and bio-sensing. Full article

An efficient redox initiating system, ceric ammonium nitrate/nitric acid, has been employed for the first time to carry out photo-induced graft copolymerization of acrylonitrile (AN) onto sodium salt of partially carboxymethylated sodium alginate, having an average degree of substitution value to be 1.10. The photo-grafting reaction conditions for maximum grafting have been systematically optimized by varying the reaction variables such as reaction time, temperature, the concentration of acrylonitrile monomer, ceric ammonium nitrate, and nitric acid, as well as the amount of the backbone. The optimum reaction conditions are obtained with a reaction time of 4 h, reaction temperature of 30 °C, acrylonitrile monomer concentration of 0.152 mol/L, initiator concentration of 5 × 10⁻³ mol/L, nitric acid concentration of 0.20 mol/L, amount of backbone of 0.20 (dry basis) and the total volume of the reaction system of 150 mL. The highest percentage of grafting (%G) and grafting efficiency (%GE) achieved are 316.53% and 99.31%, respectively. The optimally prepared graft copolymer, sodium salt of partially carboxymethylated sodium alginate-g-polyacrylonitrile (%G = 316.53), has been hydrolyzed in an alkaline medium (0.7N NaOH, 90–95 °C for ~2.5 h) to obtain the superabsorbent hydrogel, H–Na–PCMSA–g–PAN. The chemical structure, thermal characteristics, and morphology of the products have also been studied. Full article

Poly(lactic acid) (PLA) is currently the most widely used material in 3D printing. PLA has good mechanical properties, chemical stability, and biodegradability, but its surface is hydrophobic and cannot be effectively used. The growth metabolism of attachments, how to increase the strength of PLA with high brittleness, and 3D printing of PLA materials for the biomedical field have always been a topic of research by scientists. This experiment used fused filament fabrication (FFF) to prepare structures. First, the 3D-printed polymer surfaces were treated with an atmospheric-pressure plasma jet (APPJ) to make the surface hydrophilic and increase the number of polar functional groups on the surface. Then, UV photo-grafting polymerization of 2-hydroxyethyl methacrylate (HEMA), poly(ethylene glycol) methacrylate (PEGMA), and hydroxyapatite (HAp) was applied onto the 3D-printed polymer surfaces. The experimental results of the water contact angle for the wettability test show that APPJ-treated and UV-grafted composite hydrogels become hydrophilic to activate the 3D-printed polymer surface successfully. For the in vitro study, the effect of APPJ treatment and composite hydrogel on the viability of osteoblast-like MG63 cells was examined using the Alamar Blue cell viability assay, indicating that biocompatibility has been improved in this study. This method is expected to have potential in the application of bone scaffolds in the future. Full article

In order to improve the flame retardancy of polyacrylonitrile (PAN) fabrics, glycidyl methacrylate (GMA) was first grafted onto the surface of PAN fabric (PAN-g-GMA) by means of UV-induced photo grafting polymerization process. Then, PAN-g-GMA was chemically grafted with chitosan to obtain a bigrafted PAN fabric (PAN-g-GMA-g-CS). Finally, the flame-retardant PAN fabric (FR-PAN) was prepared by phosphorylation. The structure and elemental analysis of the samples were characterized by Fourier transform infrared spectroscopy (FTIR) and X-ray photoelectron spectroscopy (XPS). The thermal degradation properties and combustion characteristics of the fabrics were accessed by thermogravimetric analysis (TG), differential scanning calorimetry (DSC), and cone calorimeter (CC). The results show that the onset thermal decomposition temperature of FR-PAN fabric is lower than that of the control sample due to the degradation of the grafting groups. The combustion test indicates that the FR-PAN fabric has an excellent flame-retardant property and the combustion rate is significantly reduced. In addition, the char residue of the burned FR-PAN fabric is over 97%, indicating excellent char-forming ability. Full article

Polylactic acid (PLA) filaments are very popular as a thermoplastic source used in the 3D printing field by the “Fused Deposition Modeling” method in the last decade. The PLA market is expected to reach 5.2 billion US dollars in 2020 for all of its industrial uses. On the other hand, 3D printing is an expanding technology that has a large economic potential in many industries where PLA is one of the main choices as the source polymer due to its ease of printing, environmentally friendly nature, glossiness and multicolor appearance properties. In this review, we first reported the chemical structure, production methods, general properties, and present market of the PLA. Then, the chemical modification possibilities of PLA and its use in 3D printers, present drawbacks, and the surface modification methods of PLA polymers in many different fields were discussed. Specifically, the 3D printing method where the PLA filaments are used in the extrusion-based 3D printing technologies is reviewed in this article. Many methods have been proposed for the permanent surface modifications of the PLA where covalent attachments were formed such as alkaline surface hydrolysis, atom transfer polymerization, photografting by UV light, plasma treatment, and chemical reactions after plasma treatment. Some of these methods can be applied for surface modifications of PLA objects obtained by 3D printing for better performance in biomedical uses and other fields. Some recent publications reporting the surface modification of 3D printed PLA objects were also discussed. Full article

Traditional methods using coupling chemistry for surface grafting of heparin onto polyurethane (PU) are disadvantageous due to their generally low efficiency. In order to overcome this problem, a quick one-step photografting method is proposed here. Three heparin derivatives incorporating 0.21, 0.58, and 0.88 wt% pendant aryl azide groups were immobilized onto PU surfaces, leading to similar grafting densities of 1.07, 1.17, and 1.13 μg/cm², respectively, yet with increasing densities of anchoring points. The most negatively charged surface and the maximum binding ability towards antithrombin III were found for the heparinized PU with the lowest amount of aryl azide/anchor sites. Furthermore, decreasing the density of anchoring points was found to inhibit platelet adhesion to a larger extent and to prolong plasma recalcification time, prothrombin time, thrombin time, and activated partial thromboplastin time to a larger extent. This was also found to enhance the bioactivity of immobilized heparin from 22.9% for raw heparin to 36.9%. This could be explained by the enhanced molecular mobility of immobilized heparin when it is more loosely anchored to the PU surface, as well as a higher surface charge. Full article

Biofilm is a significant cause for membrane fouling. Antibacterial-coated surfaces can inhibit biofilm formation by killing bacteria. In this study, polyethersulfone (PES) microfiltration membrane was photografted by four antibiotic quaternary ammonium compounds (QACs) separately, which were synthesized from dimethylaminoethyl methacrylate (DMAEMA) by quaternization with butyl bromide (BB), octyl bromide (OB), dodecyl bromide (DB), or hexadecyl bromide (HB). XPS, ATR-FTIR, and SEM were used to confirm the surfaces’ composition and morphology. After modification, the pores on PES-g-DMAEMA-BB and PES-g-DMAEMA-OB were blocked, while PES-g-DMAEMA-DB and PES-g-DMAEMA-HB were retained. We supposed that DMAEMA-BB and DMAEMA-OB aggregated on the membrane surface due to the activities of intermolecular or intramolecular hydrogen bonds. Bacteria testing found the antibacterial activities of the membranes increased with the length of the substituted alkyl chain. Correspondingly, little bacteria were observed on PES-g-DMAEMA-DB and PES-g-DMAEMA-HB by SEM. The antifouling properties were investigated by filtration of a solution of Escherichia coli. Compared with the initial membrane, PES-g-DMAEMA-DB and PES-g-DMAEMA-HB showed excellent anti-biofouling performance with higher relative flux recovery (RFR) of 88.3% and 92.7%, respectively. Thus, surface functionalization of the PES membrane with QACs can prevent bacteria adhesion and improve the anti-biofouling activity by the contact-active antibacterial property. Full article

The use of a centrifugal microfluidic platform is an alternative to classical chromatographic procedures for radiochemistry. An ion-exchange support with respect to the in situ light-addressable process of elaboration is specifically designed to be incorporated as a radiochemical sample preparation module in centrifugal microsystem devices. This paper presents a systematic study of the synthesis of the polymeric porous monolith poly(ethylene glycol methacrylate-co-allyl methacrylate) used as a solid-phase support and the versatile and robust photografting process of the monolith based on thiol-ene click chemistry. The polymerization reaction is investigated, varying the formulation of the polymerisable mixture. The robustness of the stationary phase was tested in concentrated nitric acid. Thanks to their unique “easy-to-use” features, centrifugal microfluidic platforms are potential successful candidates for the downscaling of chromatographic separation of radioactive samples (automation, multiplexing, easy integration in glove-boxes environment, and low cost of maintenance). Full article

Active food packaging involves the packaging of foods with materials that provide an enhanced functionality, such as antimicrobial, antioxidant or biocatalytic functions. This can be achieved through the incorporation of active compounds into the matrix of the commonly used packaging materials, or by the application of coatings with the corresponding functionality through surface modification. The latter option offers the advantage of preserving the packaging materials’ bulk properties nearly intact. Herein, different coating technologies like embedding for controlled release, immobilization, layer-by-layer deposition, and photografting are explained and their potential application for active food packaging is explored and discussed. Full article