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The exothermic nature of acrylate photopolymerizations enables room temperature 3D printing of a quaternary formulation that incorporates an acrylate monomer, and an epoxy/thiol‐ene system (ETES). The latter comprises an epoxy monomer, a multifunctional thiol and a tetraallyl functionalized ditertiary amine curing agent. Pristine ETES necessitates temperatures of 85–95 °C for curing. Several mechanisms operate simultaneously during this process: homopolymerization of acrylates, thiol‐acrylate photopolymerization, thiol‐ene photopolymerization between the double bonds of curing agent and the multifunctional thiol, the Michael addition between thiolates derived from ETES and the double bonds of acrylates, and the anionic polymerization of the epoxy resin via the tertiary amine groups. To optimize the quaternary formulations for printing, parameters, such as reactivity, exothermicity, and viscosity, was explored. Subsequently, the thermal and viscoelastic properties of the printed cross‐linked polymers derived from these formulations were analyzed using Differential Scanning Calorimetry (DSC), Dynamic Mechanical Analysis (DMA) and Thermogravimetric Analysis (TGA). The polymers derived from quaternary formulations exhibited lower crosslinked density compared to those obtained from the pristine acrylates. This reduction in crosslink density contributes to the improved toughness of the hybrid polymers. [ABSTRACT FROM AUTHOR]

Stepwise photopolymerization is a miraculous strategy modulating the polymer skeleton and electro-optical properties of light modulators based on liquid crystal/polymer composites. However, owing to the indistinct polymerization mechanism and curing condition discrepancy, the required polymer structures and electro-optical properties are hard to be controlled precisely. Herein, a novel polymer-stabilized liquid crystal film based on acrylate/epoxy resin is proposed, fabricated and the relationships between preparation process, polymer content, polymer morphology and electro-optical properties are studied. The in-situ photopolymerization of acrylate/epoxy resin liquid crystalline polymer is fulfilled using cation photo-initiator UV 6976. The distinct photopolymerization speed between acrylate and epoxy resin benefits the polymer morphology control, and with accurate containment of the polymerization process and polymer composition, the superior electro-optical properties at a higher polymer content are acquired. The polymer morphology and electro-optical properties are influenced by the polymer content and mass ratio between acrylate and epoxy resin. The best electro-optical properties among samples are attained by controlling the mass ratio between acrylate and epoxy resin to 1:1, integrating higher densities of scattering centers and lower anchoring effect. With higher polymer content, the strategy of increasing the mass ratio of E6M benefits the improvement of E-O properties for alleviating polymer density. This work provides insights to stepwise polymerization of liquid crystalline monomers and offers a fancy strategy for the preparation of novel liquid crystal dimming films. [ABSTRACT FROM AUTHOR]

The list of standard abbreviations for JDS is available at adsa.org/jds-abbreviations-24. Nonstandard abbreviations are available in the Notes. Dietary methane (CH 4) mitigation is in some cases associated with an increased hydrogen (H 2) emission. The objective of the present study was to investigate the acute and short-term effects of acceptors for H 2 (fumaric acid, acrylic acid, or phloroglucinol) supplemented via pulse-dosing to dairy cows fed CH 4 mitigating diets (using nitrate or 3-nitrooxypropanol), on gas exchange, rumen gas, and VFA composition. For this purpose, 2 individual 4 × 4 Latin square experiments were conducted with 4 periods of 3 d (nitrate supplementation) and 7 d (3-nitrooxypropanol supplementation), respectively. In each study, 4 rumen-cannulated Danish Holstein cows were used. Each additive for CH 4 mitigation was included in the ad libitum–fed diet within the 2 experiments (exp. 1 and exp. 2), to which the cows were adapted for at least 14 d. Acceptors for H 2 were administered twice daily in equal portions through the rumen fistula immediately after feeding of the individual cow. In exp. 1 (nitrate), the treatments were CON-1 (no H 2 -acceptor), FUM-1 (fumaric acid), ACR-1 (acrylic acid), and FUM+ACR-1 (50% FUM-1 + 50% ACR-1). In exp. 2 (3-nitrooxypropanol), the 3 treatments, CON-2, FUM-2, and ACR-2, were similar to CON-1, FUM-1 and ACR-1 treatments, however the fourth treatment was PHL-2 (phloroglucinol). Gas exchanges were measured in respiration chambers, and samples of rumen liquid and headspace gas were taken in time series relative to feeding and dosing on specific days. Headspace gas was analyzed for gas composition, and rumen liquid was analyzed for VFA composition and dissolved gas concentrations. Headspace gas composition and dissolved gas concentration were only measured in exp. 2. Dry matter intake was reduced upon acrylic acid supplementation. There were no significant effects of any treatments in any experiments on H 2 emission, except for a decrease in hourly H 2 emission rate (g/h) at 1 h after feeding in both experiments. In exp. 2, H 2 headspace proportions increased with ACR-2 supplementation, whereas dissolved concentrations were unaffected. In exp. 1, cows on ACR-1 increased propionate proportion at 1 h after feeding. In exp. 2, both FUM-2 and ACR-2 increased rumen propionate proportion in the hours after feeding and dosing. There was no effect on rumen acetate for cows on PHL-2. There was a strong positive correlation between rumen dissolved CH 4 and headspace CH 4 (r = 0.84), whereas the equivalent correlation was weaker for H 2 (r = 0.41). For the relationship between dissolved concentrations and emissions of CH 4 and H 2 , there was a moderate positive correlation for CH 4 (r = 0.54), whereas it was weak for H 2 (r = 0.28) with zero slope. In conclusion, the results suggested that fumaric acid and acrylic acid to some extent was reduced to propionate without associative effects on measures for H 2 redirection. Furthermore, phloroglucinol seemed not to be metabolized in the rumen in the present study, because no effects on rumen acetate or measures of H 2 were observed. Changes in H 2 headspace and emission may be a poor proxy for actual changes in the rumen fluid concentration of H 2. [ABSTRACT FROM AUTHOR]

A new type of UV-curable pressure-sensitive adhesive containing Si atoms (Si-PSAs) was prepared by a solution-free UV-initiated telomerization process of n-butyl acrylate, acrylic acid, methyl methacrylate, and 4-acrylooxybenzophenone using triethylsilane (TES) as a telogen and an acylphosphine oxide (APO) as a radical photoinitiator. Selected commercial adhesion promoters were tested as additives in the formulation of adhesive compositions, i.e., (i) an organic copolymer with polar groups (carboxyl and hydroxyl); (ii) a hydroxymetal-organic compound; and (iii) a quaternary ammonium salt and (iv) a chlorinated polyolefin. No fillers, crosslinking agents, or photoinitiators were used in the adhesive compositions. NMR techniques confirmed the incorporation of silicon atoms into the polyacrylate structure. The influence of adhesion promoters on the kinetics of the UV-crosslinking process of Si-PSAs was investigated by a photo-DSC technique. The obtained Si-PSAs were characterized by adhesion (to steel, glass, PMMA, and PE), tack, and cohesion at 20 °C. Finally, the wetting angle of Si-PSAs with water was checked and their thermal stability was proved (TGA). Unexpectedly, the quaternary ammonium salt had the most favorable effect on improving the thermal stability of Si-PSAs (302 °C) and adhesion to glass and PMMA. In contrast, Si-PSAs containing the hydroxymetal-organic compound showed excellent adhesion to steel. [ABSTRACT FROM AUTHOR]

The current study focuses on the synthesis of a new organic compound namely, ethyl 2-benzoyl-3,3-bis(methylthio)acrylate, whose structural characterization was performed by single-crystal X-ray analysis. The central portion of the title molecule is planar. The benzoyl and one methylthio group are perpendicular to this plane while the ester and the other methylthio group lie close to the plane. In the crystal, C–H···O hydrogen bonds form chains along the b-axis direction which pack with normal Van der Waals interactions. A Hirshfeld surface (HS) analysis showed H⋅⋅⋅H contacts account for 48.3% of the intermolecular contacts in the crystal packing. The energy framework analysis shows that the contribution of dispersion forces in crystal packing is dominant among other energies. The density functional theory (DFT) study using the 6–31 + G(d,p) basis set provides further insight into reactivity and electronic and optical properties in the gas phase. The HOMO–LUMO gap for the title compound is small which indicates its soft nature and high reactivity. Natural population analysis (NPA) reveals excellent charge transfer and donor–acceptor properties in the compound. The computed global reactivity descriptors also indicate the electronic stability and reactivity of the structure. Molecular electrostatic potential (MESP) map suggested electron-rich sites around the carbonyl (C = O) and oxygen atoms while the corner carbon atoms of the benzene ring are suitable for nucleophilic attack. Furthermore, the significant dipole moment (µo) and polarizability (αo) suggest its high polarizability and optical properties. The measured static first hyperpolarizability (βo) value of 266.74 au indicates its nonlinear optical (NLO) properties. [ABSTRACT FROM AUTHOR]

AbstractInspired by leaf lotus effect, superhydrophobic surfaces have developed rapidly in recent years. In this paper, anatase nano TiO2 with particles size of about 70 nm was successfully loaded on the surface of SiO2 by sol-gel method. SiO2 and TiO2 were chemically bonded by Ti-O-Si and constructed a certain micro- and nano-composite structure. After superhydrophobic composite PA-TiO2@SiO2 was obtained by copolymerizing with acrylate and other monomers. The coating was prepared by drop coating plus spraying coating on glass substrates with water contact angles >160° and excellent self-cleaning properties, which could maintain the performance of the superhydrophobic coating by immersion in acidic solutions or water for 2 days. Meanwhile, the coating on the surface of the glass plate at −20 °C significantly delayed the freezing time of the ice. The rough structure of the surface and the presence of fluorine-containing hydrophobic groups gave the superhydrophobic coating an advantage over acrylate polymers in reducing the corrosion rate of steel surfaces. [ABSTRACT FROM AUTHOR]

Iridium catalyzed electrochemical coupling of naphthols with acrylates for the syntheses of naphtho[1,8‐bc]furan derivatives are herein reported. Ir‐catalyzed electrochemical C−H annulation is accomplished within a supportive catalysis manifold, paving the way for electrooxidative C−H acrylation via weak O‐coordination. The merge of iridium catalysts and electric current not only minimizes the need for a stoichiometric amount of chemical oxidants but also confirms broad reaction compatibility with a variety of electronically and sterically diverse substrates. This utility provides a valuable method for producing a wide range of naphtho[1,8‐bc]furan derivatives in good to moderate yields. [ABSTRACT FROM AUTHOR]

Block copolymers, comprising polyether and polyolefin segments, are an important and promising category of functional materials. However, the lack of efficient strategies for the construction of polyether‐b‐polyolefin block copolymers have hindered the development of these materials. Herein, we propose a simple and efficient method to obtain various block copolymers through the copolymerization of epoxides and acrylates via bimetallic synergistic catalysis. The copolymerization of epoxides and acrylates proceeds in a sequence‐controlled manner, where the epoxides‐involved homo‐ or copolymerization occurs first, followed by the homopolymerization of acrylates initiated by the alkoxide species from the propagating polymer chain, thus yielding copolymers with a block structure. Notably, the high monomer compatibility of this powerful strategy provides a platform for synthesizing various polyacrylate‐based block copolymers comprising polyether, polycarbonate, polythiocarbonate, polyester, and polyurethane segments, respectively. [ABSTRACT FROM AUTHOR]

By the optimization of previously established pancreatic lipase (PL) inhibitory lead, we have developed novel chromone‐containing analogues with embedded acrylate fragment as potential PL inhibitors. The analogues were designed by considering the structural features required for binding at the active site of PL enzyme with the utilization of molecular docking study. An optimized synthetic scheme was utilized for the synthesis of designed analogues of prototypes 1&2. Through in vitro PL inhibitory screening, three analogues namely, 5fj, 5gj and 9a were identified as potent PL inhibitory leads with IC50 values of 4.92, 4.23 and 3.32 μM, respectively. The protein binding of analogue 9a was analysed by fluorescence quenching study and it was found to bind at one binding site with a binding constant of 1.93 × 105 L mol−1. Analogue 9a also exhibited a competitive inhibitory mechanism with Ki value of 1.601 μM. In future, the potent lead 9a can be optimized to get a comparable or more potential PL inhibitory activity than marketed drugs. [ABSTRACT FROM AUTHOR]

Acrylates/acrylic acid are important for polymer industry due to its very high volume applications in different sectors. Activity of Ba/Mg modified hydroxyapatite for vapour-phase dehydration of ammonium lactate with 100% conversion and 60% acrylate selectivity was attributed to fine tuning of acid/base properties and formation of surface Ba/Ca lactate species. [ABSTRACT FROM AUTHOR]

Depending on the clinical context, objectives, and treatment requirements, a variety of prosthetic devices capable of artificially reconstructing the dental arches in a manner as customized as possible can be utilized in the treatment of complete edentation. The purpose of this study is to compare the efficacy of general vitamin B12 treatment vs the efficacy of local treatment accomplished through full dentures. The study was performed on a group of patients of Dental Faculty in Iasi.Because cyanocobalamin deficiency is typically treated parenterally, the current study proved the superiority of local treatment with complete dentures obtained through the crosslinked polymerization method, a much easier and less expensive way to perform the same treatment in the same time period.

Stepwise photopolymerization is a miraculous strategy modulating the polymer skeleton and electro-optical properties of light modulators based on liquid crystal/polymer composites. However, owing to the indistinct polymerization mechanism and curing condition discrepancy, the required polymer structures and electro-optical properties are hard to be controlled precisely. Herein, a novel polymer-stabilized liquid crystal film based on acrylate/epoxy resin is proposed, fabricated and the relationships between preparation process, polymer content, polymer morphology and electro-optical properties are studied. The in-situ photopolymerization of acrylate/epoxy resin liquid crystalline polymer is fulfilled using cation photo-initiator UV 6976. The distinct photopolymerization speed between acrylate and epoxy resin benefits the polymer morphology control, and with accurate containment of the polymerization process and polymer composition, the superior electro-optical properties at a higher polymer content are acquired. The polymer morphology and electro-optical properties are influenced by the polymer content and mass ratio between acrylate and epoxy resin. The best electro-optical properties among samples are attained by controlling the mass ratio between acrylate and epoxy resin to 1:1, integrating higher densities of scattering centers and lower anchoring effect. With higher polymer content, the strategy of increasing the mass ratio of E6M benefits the improvement of E-O properties for alleviating polymer density. This work provides insights to stepwise polymerization of liquid crystalline monomers and offers a fancy strategy for the preparation of novel liquid crystal dimming films.

With the rapid development of the 3D printing technique, the concept of 4D has emerged, defining time as the fourth dimension. This concept allows for changes in the appearance, function, or other properties of 3D printed objects in response to certain controlled external stimuli over time. In this work, a new photocomposite containing fluorescein based is designed on an interpenetrating polymer network (IPN) system, this system can be generated by the simultaneous photopolymerization of acrylate and epoxide monomers under visible LED@405 nm irradiation. Unexpectedly, combining the reversible fluorometric turn‐on property of fluorescein and the deformation of the IPN in the presence of water, the 3D flower structure printed from this photocomposite would demonstrate a novel dual responsive behavior with both fluorescence and shape changes when it is exposed to water for a short time. This work would present a novel functional photocomposite material and also expand the application prospect of 4D printing. [ABSTRACT FROM AUTHOR]

Double-layered polymer-stabilised cholesteric liquid crystal (PSCLC) films constructed from epoxy resin and polyacrylate were prepared based on photopolymerisation-induced phase separation. Moreover, a PSCLC film with an interpenetrating network was prepared through a one-step photopolymerisation approach. A colourful pattern was prepared based on these two approaches, which was suitably applied for decoration. [ABSTRACT FROM AUTHOR]

Antibacterial hydrogels, as an advanced approach, can create optimal conditions for wound healing, even in the fight against stubborn and difficult‐to‐treat wound infections. Interestingly, pH is an often neglected clinical parameter, although it has a significant impact on the wound healing process. At different stages of wound healing, the pH in the wound bed changes from slightly alkaline to neutral to acidic. To develop novel pH‐sensitive antibacterial hydrogel dressings, Zn2+‐loaded poly(2‐hydroxyethyl acrylate/itaconic acid) hydrogels are synthesized. The hydrogels exhibit pH‐sensitive swelling in the physiologically relevant pH range, with a pronounced swelling ability at neutral pH. The controlled release of Zn2+ occurs in a buffer of pH 7.40 at 37 °C. The liquid transport mechanism and release kinetics are evaluated using the specific kinetic models of Ritger‐Peppas and Peppas‐Sahlin. The effect of Zn2+ on structural, thermal, swelling, cytocompatibility, and antibacterial properties is evaluated by Fourier transform infrared spectroscopy, differential scanning calorimetry, swelling studies, MTT, and antibacterial tests. The hydrogels show excellent antibacterial activity against Escherichia coli. The research opens new perspectives for efficient wound healing management, and the extension of the study will be orchestrated by optimising the hydrogel composition to achieve improved performance. [ABSTRACT FROM AUTHOR]

Quantum dots (QDs), with their exceptional optical properties, have emerged as promising candidates to replace traditional phosphors in lighting and display technologies. This study delves into the integration strategies of QDs within glass and polymer matrices to engineer advanced quantum dot color converters (QDCCs) at the industrial scale for practical applications. To achieve enhancements in the photostability and thermal stability of QDCCs, we explore two distinct approaches: the dispersion of QDs in a hydrophilic glass matrix via a sol–gel process and the incorporation of QDs into a non-polar acrylate monomer to formulate QD/polymer nanocomposites. This research further investigates the optical behaviors of these composites, focusing on their light-scattering and propagation mechanisms, which are critical for optimizing light extraction efficiency in QDCCs. Additional optical film and light-scattering particles can improve color conversion efficiency by ~140%. These advancements present a significant step forward in the development of high-performance, energy-efficient, QD-based lighting and display systems. [ABSTRACT FROM AUTHOR]

The use of superabsorbent polymers (SAPs) in dryland agricultural areas utilizing brackish irrigation water is a strategy to increase plant available water (AW). However, water retention by SAPs may be adversely affected under salinity. SAP containing calcium carbonate (Ca-SAP) is considered to be more resistant and provide more plant AW under saline conditions compared to conventional SAP (C-SAP) and to control. This research investigated two replicated lettuce trials to evaluate three treatments (Ca-SAP, C-SAP and control) subjected to irrigation water with electrical conductivities of 0.0, 0.5, 1.0, 2.0 and 4.0 dS m−1. Both SAP treatments increased AW by an average of 0.16 m3 m−3 as compared to the control. Decrease in AW with salinity was lower in Ca-SAP (0.07 m3 m−3) as compared with C-SAP (0.13 m3 m−3). Lettuce fresh weight (g plant−1) was higher for Ca-SAP (22.9) as compared to C-SAP (16.4), however, did not differ from control (20.6). As water salinity increased, lettuce fresh biomass was higher in Ca-SAP as compared to C-SAP up to 2 dS m−1 with no significant differences from control. The Ca-SAP is less affected by salts than the C-SAP, although its use did not benefit lettuce growth under saline conditions as expected. [ABSTRACT FROM AUTHOR]

A practical acrylate oligomer was prepared with bisphenol A epoxy resin (CYD-128), ethylene glycol diglycidyl ether (EP-669) and acrylic acid (AAc) as the main raw materials as well as with p-hydroxyanisole as an inhibitor and tetraethyl-ammonium bromide as a catalyst. The main factors affecting the reaction, such as reaction temperature, polymerization inhibitors and catalysts, were studied. It was found that the optimal preparation reaction conditions were that reactive temperature was 90 °C-110 °C, mass fraction of p-hydroxyanisole was 0.20%-0.40%, and mass of tetraethyl ammonium bromide was 0.80%. Benzoin dimethyl ether (BDK) was directly added to the practical acrylate oligomer to prepare an UV-curable resin. The tensile mechanical properties of its UV-cured splines were tested. The experimental results showed that the tensile strength of the UV cured tensile splines was 21.3 MPa, the Young's modulus was 683.5 MPa, and the elongation at break was 7.9%. [ABSTRACT FROM AUTHOR]

Copyright of Silicone Material is the property of Silicone Material Editorial Office and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

VenaSealTM is composed of a cyanoacrylate adhesive compound often utilized for chronic venous stasis treatment. Rare case reports of hypersensitivity reactions to this compound exist. We present the first case of dermatographism and angioedema after utilization of VenaSealTM successfully treated via high dose antihistamines. We also present a case of type IV hypersensitivity to VenaSealTM, a cyanoacrylate, occurring in a patient with known meth(acrylate) allergy indicating a possible cross reactivity between these acrylate groups. [ABSTRACT FROM AUTHOR]

A new type of UV-curable pressure-sensitive adhesive containing Si atoms (Si-PSAs) was prepared by a solution-free UV-initiated telomerization process of n-butyl acrylate, acrylic acid, methyl methacrylate, and 4-acrylooxybenzophenone using triethylsilane (TES) as a telogen and an acylphosphine oxide (APO) as a radical photoinitiator. Selected commercial adhesion promoters were tested as additives in the formulation of adhesive compositions, i.e., (i) an organic copolymer with polar groups (carboxyl and hydroxyl); (ii) a hydroxymetal-organic compound; and (iii) a quaternary ammonium salt and (iv) a chlorinated polyolefin. No fillers, crosslinking agents, or photoinitiators were used in the adhesive compositions. NMR techniques confirmed the incorporation of silicon atoms into the polyacrylate structure. The influence of adhesion promoters on the kinetics of the UV-crosslinking process of Si-PSAs was investigated by a photo-DSC technique. The obtained Si-PSAs were characterized by adhesion (to steel, glass, PMMA, and PE), tack, and cohesion at 20 °C. Finally, the wetting angle of Si-PSAs with water was checked and their thermal stability was proved (TGA). Unexpectedly, the quaternary ammonium salt had the most favorable effect on improving the thermal stability of Si-PSAs (302 °C) and adhesion to glass and PMMA. In contrast, Si-PSAs containing the hydroxymetal-organic compound showed excellent adhesion to steel.

Acrylate is a popular polymer grouting material that has been widely used to control groundwater seepage. However, the vulnerability of acrylate slurry to dynamic water washout restricts its application in groundwater environments characterized by high flow velocity and water pressures. In this paper, lithium bentonite (Li-B) was used to modify the traditional magnesium acrylate (AC) grouting material. The influence of Li-B to AC ratios on the modified materials' washout resistance was explored, and the modification mechanism was analyzed using X-ray diffraction (XRD), infrared spectroscopy (IR), and scanning electron microscopy (SEM). Finally, the anti-washout ability of the modified slurry was verified through engineering applications. Results revealed that LiB-AC grout had adjustable setting times (10.5 to 395.6 s), minimal bleeding (0.1%), higher viscosity (65 mPa·s) and expansibility (350%), stronger anti-water dispersibility (24 times that of pure AC slurry), higher mechanical strength (compressive strength is 0.386 MPa, tensile strength is 0.088 MPa), and better impermeability (2.23 × 10−8 m/s). The lithium bentonite was beneficial to the setting time, bleeding, viscosity, slurry retention rate, impermeability, and mechanical strength of the acrylate grout. However, it diminished the expansibility of the acrylate grout. At the optimal acrylate content (20%), the mechanical strength and impermeability of the LiB-AC grout were the highest. The better performance of LiB-AC grout was attributed to the formation of a more stable and dense interlaced spatial network structure after the modification by Li-B. The LiB-AC grout was used in the dynamic water grouting project of a metro shield tunnel segment and achieved better anti-washout performance than cement-water glass and pure AC slurry. [ABSTRACT FROM AUTHOR]

Depending on the clinical context, objectives, and treatment requirements, a variety of prosthetic devices capable of artificially reconstructing the dental arches in a manner as customized as possible can be utilized in the treatment of complete edentation. The purpose of this study is to compare the efficacy of general vitamin B12 treatment vs the efficacy of local treatment accomplished through full dentures. The study was performed on a group of patients of Dental Faculty in Iasi.Because cyanocobalamin deficiency is typically treated parenterally, the current study proved the superiority of local treatment with complete dentures obtained through the crosslinked polymerization method, a much easier and less expensive way to perform the same treatment in the same time period. [ABSTRACT FROM AUTHOR]

Acrylic materials exhibit favorable grouting repair performance. However, their curing products are easily inclined to drying shrinkage, and their concrete impermeability repair characteristics have seldom been investigated. To improve material properties, reveal the impermeability repair mechanism, and address drying shrinkage, this study proposed the addition of styrene–acrylate copolymer emulsion (styrene–acrylic emulsion) to the grouting material to prepare two-component acrylate grouting materials. Using orthogonal and single-factor tests combined with physical and mechanical properties, the mechanical properties and impermeability repair performance (physical and mechanical properties combined) of grouting materials were analyzed and studied, and the optimal ratio of each component of acrylate grouting materials was determined. Results show that (1) the hydrogel produced by the reaction of sodium methacrylate with hydroxyethyl acrylate has good physical and mechanical properties. (2) With the increase in the accelerator dosage, the setting time of slurry initially decreases and then increases; as the initiator dosage increases, the setting time of slurry decreases, which is negatively correlated with the initiator dosage. (3) Talcum powder can improve the physical and chemical properties of gel and enhance the reliability and durability of acrylate grouting materials, and the comprehensive performance is the best at a dosage of 3%. (4) Styrene–acrylic emulsion can increase the solid content and reduce the volume drying shrinkage when added to grouting materials. The fractured impermeable specimens were repaired by grouting with prepared acrylate grouting materials and cured for 24 h for the impermeability test, and the water pressure for the 24 h impermeability repair was 1.0 MPa. This study's results provide important reference and basis for revealing the impermeability principle of acrylate grouting materials and evaluating their impermeability. [ABSTRACT FROM AUTHOR]

A high molecular flame retardant and dust inhibitor lotion was synthesized from 9,10-dihydn> 9-oxa-10-phaphenanthroline-10-oxide (DOPO), vinyl trimeth oxy silane (YDH-171), methyl methacrylate (MMA), butyl acrylate (BA), sodium dodecyl sulfate (SDS) and alkylphenol polyoxyethylene ether (OP-10) by traditional free radical polymerization. The structure of the product was characterized by FTIR, SEM and TGA, and its water retention, wind erosion resistance, rain resistance and compression resistance were tested. The results show that the prepared lotion is stable, the particle size distribution is uniform, and the film is flexible after drying. The water retention, wind erosion resistance, rain resistance and compression resistance of coal samples treated with flame retardant and dust suppressant have been significantly improved compared with raw coal samples. [ABSTRACT FROM AUTHOR]

We show here brand-new possibilities of lab-in-lab fabrication while combining holographic photopolymerization and microfluidics. One shot real-time 3D-printing can produce 3D architectured microchannels, or free-standing complex micro-objects eventually in flow. The methodology is very versatile and can be applied to e.g., acrylate resins or hydrogels.

The effect of semiconducting tungsten disulfide (WS2) nanoparticles (NPs), functionalized by either methacryloxy, glycidyl, vinyl, or amino silanes, has been studied in photocuring of acrylate and epoxy resins (the latter photocured according to a cationic mechanism). The curing time, degree of curing (DC), thermal effects, and mechanical properties of the radiation-cured resins were investigated. X-ray photoelectron spectroscopy (XPS) and transmission electron microscopy (TEM) analyses confirmed that a silane coating was formed (1–4 nm) on the NPs' surface having a thickness of 1–4 nm. Fourier transition infrared (FTIR) was used to determine the DC of the nanocomposite resin. The curing time of the epoxy resin, at 345–385 nm wavelength, was 10 to 20 s, while for acrylate, the curing time was 7.5 min, reaching 92% DC in epoxy and 84% in acrylate. The glass transition temperature (Tg) of the photocured acrylates in the presence of WS2 NPs increased. In contrast to the acrylate, the epoxy displayed no significant variations of the Tg. It was found that the silane surface treatments enhanced the DC. Significant increases in impact resistance and enhancement in shear adhesion strength were observed when the NPs were treated with vinyl silane. A previous study has shown that the addition of WS2 NPs at a concentration of 0.5 wt.% is the optimal loading for improving the resin's mechanical properties. This study supports these earlier findings not only for the unmodified NPs but also for those functionalized with silane moieties. This study opens new vistas for the photocuring of resins and polymers in general when incorporating WS2 NPs. [ABSTRACT FROM AUTHOR]

Investigations of historical conservation materials on historical stained glass windows of the Naumburg Cathedral in Germany offered an opportunity for the study of polymers, naturally aged in a non-controlled environment. This allowed the conservation history of the cathedral to be traced and expanded by valuable insights. The historical materials were characterized through the use of spectroscopy (FTIR, Raman), thermal analysis, PY-GC/MS, and SEC on taken samples. The analyses show that acrylate resins were predominantly used for conservation. The lamination material from the 1940s is particularly noteworthy. Epoxy resins were also identified in isolated cases. Artificial aging was used to investigate the influence of environmental influences on the properties of the identified materials. Through a multi-stage aging program, influences of UV radiation, high temperatures and high humidity can be considered in isolation. Piaflex F20, Epilox, Paraloid B72 as a modern material and combinations of Paraloid B72/diisobutyl phthalate and PMA/diisobutyl phthalate were investigated. The parameters yellowing, FTIR spectra, Raman spectra, molecular mass and conformation, glass transition temperature, thermal behavior, and adhesive strength on glass were determined. The effects of the environmental parameters on the investigated materials are differentiated. UV and extreme temperatures tend to show a stronger influence than humidity. The comparison of the artificially aged samples with the naturally aged samples from the cathedral shows that the latter were less aged. Recommendations for the conservation of the historical stained glass windows were derived from the results of the investigation. [ABSTRACT FROM AUTHOR]

Copyright of Polymer Materials Science & Engineering is the property of Sichuan University, Polymer Research Institute and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Copyright of Coal Geology & Exploration is the property of Xian Research Institute of China Coal Research Institute and its content may not be copied or emailed to multiple sites or posted to a listserv without the copyright holder's express written permission. However, users may print, download, or email articles for individual use. This abstract may be abridged. No warranty is given about the accuracy of the copy. Users should refer to the original published version of the material for the full abstract. (Copyright applies to all Abstracts.)

Functional textiles are widely concerned because of their potential applications in various fields, water-repellent textiles play a vital role in functional textiles because of their huge practical needs. However, the realization of water-repellent finishing agent with high stability and heat resistance has remained an open challenge, limiting the further application of water-repellent textiles. Herein, waterborne polyurethane (WPU) is prepared by introducing C = C bonds into polyurethane (PU) side chains using trimethylolpropane monoallyl ether (TMPME) as a grafting agent by self-emulsification. As a seed emulsion, WPU is further copolymerized with acrylate monomers to prepare waterborne polyurethane/acrylate (WPUA). Interestingly, the WPUA emulsions with obvious core–shell structure exhibit excellent storage stability and heat resistance, which can cover the fabric surface and form a thin film. The static contact angle up to 151° imparts excellent water repellency to the fabric. Thus, a water-repellent finishing agent was successfully assembled, which possesses high reference value for designing and preparing such materials. [ABSTRACT FROM AUTHOR]

The development of polymeric optical materials with a higher refractive index, transparency in the visible spectrum region and easier processability is increasingly desirable for advanced optical applications such as microlenses, image sensors, and organic light-emitting diodes. Most acrylates have a low refractive index (around 1.50) which does not meet the high performance requirements of advanced optical materials. In this research, three novel acrylates were synthesized via a facile one-step approach and used to fabricate optical transparent polymers. All of the polymers reveal good optical properties including high transparency (≥90%) in the visible spectrum region and high refractive index values (1.6363) at 550 nm. Moreover, nanostructures of these acrylate polymers with various feature sizes including nanogratings and photonic crystals were successfully fabricated using nanoimprint lithography. These results indicate that these acrylates can be used in a wide range of optical and optoelectronic devices where nanopatterned films with high refractive index and transparency are required.

Waterborne coatings have obtained more and more attention from researchers with increasing concerns in environmental protection, and have the advantages of being green, environmentally friendly and safe. However, the introduction of hydrophilic groups leads to lower hydrophobicity and it is difficult to meet the requirements of complex application environments. Herein, we proposed an optimization approach of waterborne polyurethane (WPU) with vinyl tris(β-methoxyethoxy) silane (A172), and it was found that the surface roughness, mechanical properties, thermal stability and water resistance of WPU will be increased to a certain extent with the addition of A172. Moreover, the hydrophobicity of the coating film is best when the silicon content is 10% of the acrylic monomer mass and the water contact angle reaches 100°, which could exceed two-thirds of the research results in the last decade. Therefore, our study can provide some theoretical basis for the research of hydrophobic polyurethane coatings. [ABSTRACT FROM AUTHOR]

Photopolymerization offers a unique opportunity to convert liquid monomers to polymers using light as the activation source. Recently, major efforts have been devoted to developing visible light photo-initiating systems, and the search for new dyes that can be incorporated into photocurable resins and polymerize a resin within a few seconds is still ongoing. With the aim of exploring a maximum of structures to reach this goal, quinoxaline has been identified to be a promising scaffold for the design of UV-centered and visible light photo-initiating systems. In this review, an overview of the different quinoxaline-based dyes will be given. In order to evidence the interest in these structures, comparisons with reference systems will be given. [ABSTRACT FROM AUTHOR]

A complex [Zn(bpy)(acr)2]·H2O (1) was converted in a DMF medium (DMF = N,N′-dimethylformamide) into a coordination polymer [Zn(bpy)(acr)(HCOO)]n (1a) (bpy = 2,2′-bipyridine, and Hacr = acrylic acid), and the species was fully characterized through a single crystal X-ray diffraction. Additional data were obtained by IR and thermogravimetric analysis. Complex (1a) crystalized the coordination polymer in the space group Pca21 of an orthorhombic system. Structural characterization revealed that Zn(II) adopted a square pyramidal stereochemistry generated by bpy molecules, coordinated by chelate, acrylate, and formate ions as unidentate and bridged, respectively. The presence of both the formate and the acrylate with different coordination modes generated two bands in ranges that were characteristic for the carboxylate vibration modes. Thermal decomposition occurs in two complex steps: it first happens via a bpy release, which is followed by an overlapped process that is associated with acrylate and formate decomposition. The obtained complex is of present interest due to the presence of two different carboxylates in its composition and situation, which is rarely reported in the literature. [ABSTRACT FROM AUTHOR]

To improve the stability of waterborne epoxy–acrylic emulsions and their comprehensive properties, such as the chemical resistance of coatings, a new research idea is proposed in this paper. First, a series of high-molecular-weight epoxy resins were synthesized with epoxy resin E-51 and bisphenol A (BPA) using benzyl triphenyl phosphine bromide as the catalyst. Then, free-radical graft copolymerization was carried out between the epoxy resin and methacrylic acid (MAA), styrene (ST), and butyl acrylate (BA) using benzoyl peroxide (BPO) as the initiator. This method ensured that the epoxy groups were retained. Finally, the carboxylic acid groups were neutralized with N,N-dimethylethanolamine (DMEA), and a stable aqueous epoxy–acrylic emulsion was obtained by high-speed dispersion in deionized water. The effects of key factors such as temperature, time, the molecular weight and dosage of epoxy resin, the dosage of MAA, the dosage of BPO, and the neutralization degree of the synthesis of emulsions and coating film properties were mainly discussed. The molecular weight and molecular weight distribution of the epoxy resin were determined by gel permeation chromatography (GPC). The epoxy resin and its graft copolymer were analyzed and characterized by Fourier-transform infrared (FTIR) spectroscopy, differential scanning calorimetry (DSC), and thermogravimetric analysis (TGA). The particle size and distribution of the emulsions were tested by laser particle size analysis. The morphology of the emulsion particles was observed by transmission electron microscopy. The results showed that the acrylic monomers (MAA, ST, and BA) were grafted onto the epoxy resin. The graft copolymers showed higher glass transition temperatures compared with those of the pure epoxy resin. TGA showed that the graft copolymer started to decompose at a high temperature before the pure epoxy resin did, and the thermal stability was slightly reduced. The prepared emulsions with a particle size of 160 nm had a storage stability of more than one year and showed excellent dilution stability, mechanical stability, and freeze–thaw stability. The emulsions were coated and cured at 150 °C for 1 h with a pencil hardness of 5 H, an adhesion of grade 1, and a flexibility of 1 mm. The water resistance was >60 days, the salt water resistance was >30 days, the acid resistance was >10 days, and the alkali resistance was >5 days. [ABSTRACT FROM AUTHOR]

It has been demonstrated that the results caused by abnormal levels of Cysteine (Cys) are not negligible in biological processes. Furthermore, mitochondria are one of the most important organelles, which not only produce cellular energy, but also participate in signal transmission, growth, death, and other biological processes. Therefore, developing an efficient fluorescent probe targeting mitochondria to detect Cys in cells is useful for clinic pathological diagnosis. In this report, a near-infrared (NIR) fluorescent probe LAA based on link-anthocyanin as fluorophore and acrylate as identification groups has been prepared. Link-anthocyanin, as an NIR-emitting fluorophore, showed favorable water solubility and strong fluorescence intensity. Acrylate, as a recognition site, exhibited intense sensitivity and selectivity to Cys. In addition, LAA had a high tendency to localize to mitochondria due to the lipophilic positive ion in the link-anthocyanin. Under the excitation of 560 nm, the probe LAA could detect Cys with high selectivity and low detection limit (37 nM) at the emission of 670 nm, which belonged to the NIR range and was beneficial for biological application. Furthermore, LAA exhibited great biocompatibility and low cytotoxicity, which could monitor Cys in mitochondria of living cells in real-time.

Quantum dots (QDs), with their exceptional optical properties, have emerged as promising candidates to replace traditional phosphors in lighting and display technologies. This study delves into the integration strategies of QDs within glass and polymer matrices to engineer advanced quantum dot color converters (QDCCs) at the industrial scale for practical applications. To achieve enhancements in the photostability and thermal stability of QDCCs, we explore two distinct approaches: the dispersion of QDs in a hydrophilic glass matrix via a sol–gel process and the incorporation of QDs into a non-polar acrylate monomer to formulate QD/polymer nanocomposites. This research further investigates the optical behaviors of these composites, focusing on their light-scattering and propagation mechanisms, which are critical for optimizing light extraction efficiency in QDCCs. Additional optical film and light-scattering particles can improve color conversion efficiency by ~140%. These advancements present a significant step forward in the development of high-performance, energy-efficient, QD-based lighting and display systems.

The aim of this study is to identify the technological peculiarities of the use of bio-acrylic materials in accordance with the clinical parameters of the case, arguing the usefulness of these biomaterials in everyday dental medical practice. A number of 25 partially mobilizable acrylic prostheses were made from different types of biomaterials following the clinical-technological algorithm specific to their type of prosthesis.The variety of clinical cases in which we used acrylic biomaterials as a result of careful analysis of all clinical factors, paraclinical, provides a clear picture of the corroboration of the general condition with local and loco-regional features of the clinical case with the chosen mobilizable therapeutic solution. Partially removable acrylic prostheses remain a viable transient therapeutic solution, in social cases taking on a long-term character managing to ensure a good quality of life through the evolved structure of new acrylic biomaterials in the context of rehabilitation of all stomatognathic system functions.

In this study, hyperbranched polyglycerol (HPG) is synthesized via ring‐opening polymerization of a glycidol monomer. An epoxy group is introduced at the end of HPG through a reaction with epichlorohydrin in a one‐pot process. The number of epoxy groups introduced increase proportional to the amount of boron‐trifluoride‐tetrahydrofuran catalyst used. In addition, acrylate‐functionalized polyglycerol (AG) is synthesized via a reaction of the epoxy group with an acrylic acid, and a maximum of 5.7 acrylate groups are introduced per molecule. AG shows photocuring behavior with the photoinitiator Irgacure 819, while viscosity is adjusted from 18 to 2947 cPs by introducing up to 80 wt% 2‐hydroxyethyl acrylate (2‐HEA). Diluted resin can cure over 97 wt% even with a short UV irradiation period of 20 s. Furthermore, hydrophilicity increases proportional to the amount of 2‐HEA added, and water absorption can be controlled in the range of 30–124 wt%. [ABSTRACT FROM AUTHOR]

In this work, we test the effectiveness of using highly transparent holographic phase reflection and transmission volume gratings based on multifunctional acrylates as linear compression and rotation sensors. The gratings are recorded in a holographic mixture based on multi-reticulated acrylate and haloalkanes. To activate the photo-polymerization process, we used a mixture of 6-oxocamphore and rhodamine 6G. The mixture is a simplified version of the mixture used in previous works and shows some interesting features mainly in connection with the different roles played by the rhodamine 6G dye at different writing wavelengths λ = 532 nm and λ = 460 nm. Regarding reflection gratings, the maximum achieved diffraction efficiency is ≈50% and their use as linear compression sensors produces a shift in the reflection peak of 2 nm. Following the removal of compression, the grating slowly returns to the initial state. Regarding transmission gratings, the maximum achieved diffraction efficiency is ≈45% and they demonstrate very high sensitivity to even small rotations in a free-standing configuration. [ABSTRACT FROM AUTHOR]

As an important part of cultural heritage, paper cultural relics have important historical, scientific and humanistic values. However, a large number of paper cultural relics are suffering from aging, mildew, yellowing, cracks, embrittlement and other threats, or are even completely damaged. To enhance the strength of paper cultural relics and prolong the life of paper cultural relics, a novel CMC-acrylate-OVPOSS graft copolymer was synthesized with carboxymethyl cellulose (CMC), methyl methacrylate (MMA), butyl acrylate (BA), hydroxyethyl methacrylate (HEMA), glycidyl methacrylate (GMA), octavinyl polyhedral oligomeric silsesquioxane (OVPOSS). The synthesized materials were analyzed by infrared spectroscopy, X-ray diffractometer, thermal analyzer and X-ray photoelectron spectroscopy. In addition, the reinforcement solution was coated on the surface of the paper, and the protective effect of the reinforcement solution on the paper was evaluated by testing the mechanical and optical properties of the paper. When the reinforcement solution with a mass concentration of 10 % was coated on the paper, the mechanical properties of the paper were greatly improved, and the gloss and whiteness were basically unchanged. [ABSTRACT FROM AUTHOR]

Cationic photo-initiated and polymerized epoxies are characterized by good adhesion, high modulus, zero volatiles, low shrinkage and living polymerization characteristics. Radiation—cured acrylate resins are characterized by rapid initial curing with increased initial strength. The combination of radiation-cured acrylates and epoxies may present advantageous attributes. Thus, the system investigated is a hybrid epoxy/methyl acrylate and three different initiators for cationic polymerization of epoxies, the radical reaction of acrylates and the thermal initiator. When incorporating additives like opaque WS2 nanoparticles (NPs), absorption of the photo radiation takes place, which may lead to low photo activity. Curing kinetics measurements revealed that the absorbing/masking effect of WS2 was insignificant, and surprisingly, the level of curing was enhanced when the WS2 NPs were incorporated. FTIR results demonstrated that covalent bonds were formed between the inorganic fullerenes (IF-WS2) and the crosslinked matrix. Viscosity measurements showed a surprising reduction of five to ten times in the low-shear viscosity upon NPs incorporation compared to neat resins. It was concluded that the decrease of viscosity by the inorganic NPs, in addition to the enhanced level of conversion, has profound advantages for structural adhesives and 3D printing resins. To the best of our knowledge, this investigation is the first to report on a radiation-induced curing system containing opaque WS2 NPs that leads to an enhanced degree of curing and reduced shear viscosity. [ABSTRACT FROM AUTHOR]

The radiation curing paradigm of opaque WS2 nanoparticle (NP)-based epoxy/acrylate nanocomposites was studied and found to exhibit both a reduction in viscosity and an enhanced degree of curing when incorporating WS2 NPs. The objective of this study was to investigate the mechanical, thermal, and physical properties of a radiation-induced and cured epoxy/acrylate blend containing 0.3 to 1.0 wt.% WS2 NPs. Experimental results indicate that the tensile toughness increased by 22% upon optimizing the NP content compared to that of WS2-free formulations. Tensile fractured surfaces with different WS2 NP contents were analyzed with a scanning electron microscope and an atomic force microscope and showed distinctive morphology depending on the WS2 NP content, supporting the results of the tensile test. The energy required to break shear adhesion specimens demonstrated an increase of up to 60% compared to that of the neat resin. The glass transition temperature determined by dynamic mechanical analysis presented similar or higher values upon WS2 NP incorporation. Furthermore, up to 80% improvement in impact strength was demonstrated when WS2 NPs were dispersed in the epoxy/acrylate blend. It was concluded that the surface chemistry and dispersion level of the WS2 NPs are the major variables affecting the macro properties of cationically radiation-cured resins and their adhesion properties. This study is the first to demonstrate the possibility for radiation-induced curing of opaque NPs based on WS2 that serve as both a reinforcement nanoparticle at low concentrations and an enhancement of the degree of curing. [ABSTRACT FROM AUTHOR]

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We report on highly transparent holographic phase transmission volume gratings recorded in the visible region at λ = 532 nm. The maximum measured diffraction efficiency is higher than 80% with a grating pitch of Λ ≈ 300 nm and a refractive index modulation Δ n ≈ 0.018. To obtain these results, we used a holographic mixture based on multi-reticulated acrylate and haloalkanes (1-bromo-butane and 1-bromo-hexane) and a synergic combination of camphore-quinone, which has a maximum absorbance at c.a. 470 nm, and R6G, here used as co-initiator, to efficiently initiate the photo-polymerization process. High transparent and high efficient holographic structures based on polymers can find applications in many research fields including integrated optics, sensors, high density data storage and security. [ABSTRACT FROM AUTHOR]