Acrylate Copolymer Research Articles

Microplastic Contamination in Landfill Leachate and Surface Water: Assessment of Wastewater Treatment Efficiency at the Nonthaburi Waste Management Center, Thailand

Microplastics (MPs), plastic particles smaller than 5 mm, have emerged as a significant environmental concern, particularly as contaminants originating from landfills. Landfills can serve as a major source of MPs, potentially releasing them into surface water through leachate. This study aims to investigate the contamination of MPs in leachate and surface water, as well as to evaluate the efficiency of landfill wastewater treatment in removing these particles. The research was conducted at the Waste Management Center of the Nonthaburi Provincial Administrative Organization, Thailand, with samples collected in June 2023. Sampling included two leachate sources, influent and effluent from the treatment system and surface water. The abundance and characteristics of MPs in each sample were analyzed. Results indicated a significant presence of MPs in leachate, with an average concentration of 173.98 pieces/L, while concentrations in influent, effluent and surface water were 38.40 pieces/L, 10.80 pieces/L and 11.33 pieces/L, respectively. MPs in all samples were predominantly in the size range of 16-100 µm, corresponding to 71.28-93.75% of the total particles. Polypropylene was the dominant polymer in leachate (69.66%) and effluent (48.94%), whereas acrylate copolymer (96.53%) and polytetrafluoroethylene (44.12%) were the major types found in influent and surface water, respectively. The wastewater treatment system of the landfill demonstrated an overall removal efficiency of 71.88% for MPs in leachate. These findings highlight the extent of MP contamination in landfill environments and the importance of improving treatment processes to mitigate their release into surrounding ecosystems.

Fibrous Foes: First Report on Insidious Microplastic Contamination in Dietary Fiber Supplements

Regular consumption of health supplements to balance dietary intake has gained popularity worldwide. One such supplement that has gained popularity among consumers is dietary fibers. Microplastic (MPs) contamination in various food products is being reported worldwide. However, there is a paucity of understanding of the occurrence of MPs in dietary supplements. This study addresses this gap by investigating the degree of MPs contamination in dietary fiber supplements. Nine commonly consumed (powder and gummy-based) over-the-counter dietary fiber supplements in Australia were tested in this study. Microscopic examination revealed the presence of MPs fibers and fragments in all the tested products. Further categorization showed that MPs particles were of various colors, including black, blue, red, green, and white. The order of polymer abundance was Polyamide > Polydiallyl Phthalate > polyethylene and polypropylene-diene > Polyurethane = Polyethylene terephthalate > Polyethylene = Ethylene acrylic acid copolymer. Among the supplements, powder-based samples had higher MPs (at the adult dosage suggested by the manufacturer) than gummy-based product. The average predicted ingestion of microplastics from these supplements (all nine samples) was 5.89 ± 2.89 particles day-1. The dietary exposure for children and adults ranged from 0.1 - 0.48 and 0.18 - 4.08 particles day-1, respectively. Based on the microplastic contamination factor (MCF), among the nine samples tested, 69.81% exhibited a moderate level, while 20.76% showed a significant level of microplastic contamination. The polymer risk index (pRi) indicates products with very high and high-risk categories. The possible sources of MPs contamination in the products were studied. To our knowledge, this is the first study to record and quantify the presence of MPs in dietary fiber supplements, which is a direct source of MPs exposure to humans via., ingestion.

Free radical copolymerization kinetics of bio-based dibutyl itaconate and n-butyl acrylate

The free radical copolymerization of dibutyl itaconate (DBI), a monomer derived from renewable resources, and n-butyl acrylate (BA) is investigated to explore the potential of incorporating itaconate monomers into commercial acrylic resins to enhance the sustainability of coating materials. Batch experiments were conducted at 50 °C and 80 °C, varying initial monomer and initiator concentrations as well as monomer compositions, with proton NMR and size exclusion chromatography used to analyze monomer conversion profiles and polymer molar mass distributions (MMDs). The data were analyzed using a kinetic model developed to guide the experimental studies and estimate key kinetic parameters controlling copolymer composition, polymerization rate and polymer MMDs. The use of the more reactive BA as comonomer significantly increases the conversion and molar mass of the resulting copolymer. Furthermore, semi-batch operating conditions similar to current industrial practice can incorporate a substantial fraction of DBI into acrylic copolymer resins, thus enhancing their sustainability profile.

Ultrasound protein-copolymer microbubble library engineering through poly(vinylpyrrolidone-co-acrylic acid) structure

HypothesisWhile albumin-coated microbubbles are routine contrast agents for ultrasound imaging, their short duration of contrast enhancement limits their use, yet can be improved by incorporating protein-copolymer hybrids into microbubble shells. The incorporation of N-vinyl-2-pyrrolidone and acrylic acid copolymer (P(VP–AA)) has been shown to enhance the performance of bovine serum albumin (BSA)-coated microbubbles. However, the impact of the copolymer structural properties on key microbubble characteristics (i.e., concentration, mean diameter and acoustic response) remains poorly understood. Therefore, we hypothesize that the copolymer structure affects its capacity to form micelle-like nanoaggregates, protein-copolymer hybrids, and microbubble shells, ultimately influencing the physicochemical and acoustic properties of the microbubbles. ExperimentsHere we evaluate the production and performance of BSA@P(VP–AA) microbubbles synthesized using a series of P(VP–AA) copolymers with –C8H17 and –C18H37 end groups and molecular weight cutoffs between 3.5 and 15 kDa. Both simulation and experimental data demonstrate that interactions between BSA and the copolymers significantly influence the performance of the resulting microbubbles across the library of 60 formulations. FindingsThe introduction of –C8H17 terminated copolymers into microbubble shells resulted in up to 200-fold higher concentration, 7-fold greater acoustic response, and 5-fold longer ultrasound contrast enhancement compared to plain BSA microbubbles. The enhanced acoustic performance was sustained during in vivo cardiac ultrasound imaging, without altering liver accumulation after copolymer introduction. These findings underscore how optimizing copolymer structure (specifically the terminal end group and molecular weight) can tailor the formation and performance of protein-copolymer-coated microbubbles, offering valuable insights for designing ultrasound contrast agents.

In Situ Formation of Acidic Comonomer during Thermal Treatment of Copolymers of Acrylonitrile and Its Influence on the Cyclization Reaction.

Binary and ternary copolymers of acrylonitrile (AN), tert-butyl acrylate (TBA), and n-butyl acrylate (BA) are synthesized through conventional radical polymerization in DMSO in the presence of 2-mercaptoethanol. The thermal behavior of binary and ternary copolymers is studied under argon atmosphere and in air. It is demonstrated that the copolymers of AN contain 1-10 mol.% of TBA split isobutylene upon heating above 160 °C, resulting in the formation of the units of acrylic acid in the chain. The carboxylic groups formed in situ are responsible for the ionic mechanism of cyclization, which starts at lower temperatures compared with pure polyacrylonitrile (PAN) or AN copolymer with BA. The activation energy of cyclization through ionic and radical mechanisms depends on copolymer composition. For the ionic mechanism, the activation energy lies in the range ca. 100-130 kJ/mole, while for the radical mechanism, it lies in the range ca. 150-190 kJ/mole. The increase in the TBA molar part in the copolymer is followed by faster consumption of nitrile groups and the evolution of a ladder structure in both binary and ternary copolymers. Thus, the incorporation of a certain amount of TBA in PAN or its copolymer with BA allows tuning the temperature range of cyclization. This feature seems attractive for applications in the production of melt-spun PAN by choosing the appropriate copolymer composition and heating mode.

Vitrimer-like elastomers with rapid stress-relaxation by high-speed carboxy exchange through conjugate substitution reaction

We report vitrimer-like elastomers that exhibit significantly fast stress relaxation using carboxy exchange via the conjugate substitution reaction of α-(acyloxymethyl) acrylate skeletons. This network design is inspired by a small-molecule model that shows the carboxy exchange reaction even at ambient temperature in the presence of 1,4-diazabicyclo[2.2.2]octane (DABCO). The acrylate and acrylic acid copolymers are cross-linked using bis[α-(bromomethyl)acrylates] and doped with 10 wt% DABCO, exhibiting processability to obtain a transparent film by hot pressing. The high-speed bond exchange in the network, validated by stress-relaxation tests, allows quick molding with household iron. In addition, the material is applied as an adhesion sheet for plastic and metal substrates. Because dynamic cross-linking with the proposed bond exchange mechanism can be implemented for any polymer bearing carboxyl pendants, our approach can be applied to versatile backbones, which must thus be meaningful in the practical sense.

New Generation of Thermoplastic Elastomers from Narrowly Dispersed All-(Meth)acrylic ABA Triblock Copolymers Made by RAFT

New Generation of Thermoplastic Elastomers from Narrowly Dispersed All-(Meth)acrylic ABA Triblock Copolymers Made by RAFT

Mechanism of dust suppressant by sodium carboxymethyl cellulose grafted acrylic copolymer

In order to inhibit dust, a substance C-PAA was synthesized by free radical polymerization using sodium carboxymethyl cellulose and acrylic acid as raw materials and ammonium persulfate as an initiator. The optimal synthesis process was determined by using a single factor experimental method. Quantum chemistry and experiments were used to investigate the chemical synthesis of C-PAA. The results indicate that the active centers of the reaction were at the OH bond of sodium carboxymethyl cellulose, where H was seized by ·SO4-, produced by ammonium persulfate, to form an alkoxyl radical. Concurrently, ·SO4- attacked acrylic acid, resulting in the breakage of the CC bond, creating a CC bond, and combining with the alkoxyl group to create a new ether group that produced the compound C-PAA. The enthalpy change and activation energy of the reaction were −178.40 KJ/mol and −22.59 KJ/mol, respectively, and the infrared absorption peaks of the newly generated fatty ether and the increase in the relative content of the ether group in the final product proved that the preparation of C-PAA was successful. In order to further improve the wetting performance of the dust suppressant, pyrene fluorescence spectrometry was used to determine the critical micelle concentration of the surfactant sodium dodecyl sulfate as 1.5 g/L, and 1.5 g/L sodium dodecyl sulfate was mixed with C-PAA to obtain the dust suppressant SC-PAA. In comparison to the H2O-lignite system, the total number of hydrogen bonds in the SC-PAA-lignite system increased from 2023 to 2405, according to the molecular dynamics results. The rationale is that C-PAA in SC-PAA has a plethora of oxygen-containing functional groups, which enable it to create more hydrogen bonds with H2O as well as amino and hydroxyl groups on the surface of lignite. Due to hydrogen bonding, the dust suppressant is able to gather more water molecules adsorbed on the surface of the lignite. It then utilizes the capillary force of the coal pores to penetrate deeply into the fissures within the coal particles, thereby enhancing the wetting impact on the lignite.

Creative synthesis of pH-dependent nanoporous pectic acid grafted with acrylamide and acrylic acid copolymer as an ultrasensitive and selective riboflavin electrochemical sensor in real samples

In current research, an innovative pectic acid was grafted with poly (acrylamide-co-acrylic acid) [PA-g-poly (AAm-co-AA)] nanoporous membrane using a free radical-mediated grafting copolymerization process. The optimized parameters for the grafting copolymerization reaction such as initiator concentration, monomer concentrations, polymerization reaction time, and temperature were studied. Additionally, the solid content, graft percentage, and conversion were calculated. The unique polymeric membrane was characterized using Fourier-transform infrared spectroscopy (FT-IR), thermal gravimetry (TG), transmission electron microscopy (TEM), and scanning electron microscopy (SEM) supported by energy dispersive X-ray spectroscopy (EDX). The formulated novel PA-g-poly (AAm-co-AA) had a nanoporous structure with a diameter of 113 nm. pH-dependent swelling and biodegradation measurements were also studied. The electrochemical characterizations of PA-g-poly (AAm-co-AA) were conducted through cyclic voltammetry (CV) and electrochemical impedance spectroscopy (EIS). Furthermore, the screen-printed electrode (SPE) was modified with pure PA and the new generation of its grafted polymeric nanoparticles to detect and quantify the concentration of riboflavin (RF) in real samples using cyclic voltammetry (CV) and differential pulse voltammetry (DPV) techniques. The modified electrode showed two linear concentration ranges from 0.01 - 2 nM and 2 – 90 nM with low detection limits (LODs) of 0.004 and 0.97 nM, respectively, demonstrating high sensitivity. Besides, the fabricated sensor exhibited more selectivity, simplicity, great reproducibility, repeatability, and good stability. Finally, the PA-g-poly (AAm-co-AA)-modified SPE based sensor was effectively used in real sample analysis of egg yolk, milk, and vitamin B2 drugs with good recovery rates.

PH‐responsive bionanocomposite pectin grafted with dimethylaminoethyl methacrylate and acrylic acid copolymer along with silver nanoparticles for breast cancer drug delivery

AbstractIn this study, we developed a pH‐responsive hydrogel membrane composed of pectin, dimethylaminoethyl methacrylate (DMAEMA), and acrylic acid (AA) through a free radical‐triggered graft copolymerization method. Freshly formed silver nanoparticles (AgNPs) produced from the reduction reaction were embedded in the produced hydrogel. Pectin‐grafted dimethylaminoethyl methacrylate and acrylic acid copolymer [poly (DMAEMA‐co‐AA)‐g‐pectin] and its bionanocomposite with AgNPs were confirmed by Fourier‐transform infrared spectroscopy (FT‐IR), scanning electron microscopy (SEM), and thermogravimetric analysis (TGA). The swelling behavior of poly (DMAEMA‐co‐AA)‐g‐pectin in solutions with diverse pH values was assessed. For use as a controlled drug delivery agent, the hydrogel was loaded with 5‐fluorouracil (5‐FU). The incorporation of AgNPs had a great impact on the entrapment efficiency of 5‐FU. At pH 7.4, nearly 48% of the 5‐FU was released in vitro from the polymeric nanocomposite within 24 h. Moreover, poly (DMAEMA‐co‐AA)‐g‐pectin and poly (DMAEMA‐co‐AA)‐g‐pectin/AgNPs presented high cytocompatibility toward normal skin fibroblast cells (BJ1), and the drug delivery system strongly inhibited human Caucasian breast adenocarcinoma cells (MCF‐7). These results demonstrated that these poly (DMAEMA‐co‐AA)‐g‐pectin/AgNPs are an excellent candidate for use in anticancer drug delivery systems.Highlights Free radical polymerization of nanocomposites incorporated with nanoparticles. Nanoparticles improve the bionanocomposites' drug loading. The developed bionanocomposites exhibit control drug release. The novel bionanocomposites acts as an excellent anticancer drug carrier.

Mechanical and Thermal Properties of Polypropylene, Polyoxymethylene and Poly (Methyl Methacrylate) Modified with Adhesive Resins

Polyoxymethylene (POM), polypropylene (PP), and poly(methyl methacrylate) (PMMA) have been blended with adhesive-grade ethylene vinyl acetate (EVA), propylene elastomer (VMX), isobutylene–isoprene rubber (IIR) and an acrylic block copolymer (MMA-nBA-MMA). The blends were prepared using a two-roll mill and injection molding. The mechanical properties of the blends, such as tensile strength, tensile modulus, elongation at maximum load, and impact resistance, were investigated. The water contact angle, melt flow rate (MFR), and differential scanning calorimetry were ascertained to evaluate the blends. The blend samples exhibited the following properties: all POM/EVA blends showed reduced crystallinity compared to neat POM; the 80% PMMA/20% MMA-nBA-MMA blend showed improved impact resistance by 243% compared to the neat PMMA. An antiplasticization effect was observed for POM/EVA 1% blends and PMMA/EVA 1% blends, with MFR reduced by 1% and 3%, respectively. The MFR of the PP/IIR 1% blend increased by 5%, then decreased below the MFR near the polymer for the remaining IIR concentrations.

A conductive ionogel with Stretchability, low hysteresis and adjustable adhesion for Air/Underwater mechanosensing

Conductive ionogels based on deep eutectic solvents (DESs) have great application potential in the field of flexible sensors. However, the development of conductive ionogels that are stable under various environmental conditions (such as high and low temperatures, air, and water) remains extremely challenging. In this work, the hydrophobic conductive ionogel BxHyIG was prepared via a one-step photoinitiated copolymerization of butyl acrylate and N-hydroxyethylacrylamide in a hydrophobic DES. The good chemical compatibility between the polymer and DES, as well as the dense and reversible ion–dipole interactions, dipole–dipole interactions and hydrogen bond interactions, endow BxHyIG with satisfactory transparency (80 %), adhesion (polystyrene: 74.56 kPa), mechanical properties (elongation at break: 578 %, tensile strength: 171.25 kPa), a low degree of hysteresis (DH=1.9 %) and conductivity (3.95 × 10-3 S m−1). Strain/pressure sensors and bioelectrodes prepared from ionogels have the characteristics of high sensitivity, fast response and excellent stability and can be used for real-time monitoring of human activities and health status in the atmosphere. In addition, the inherent hydrophobicity of BxHyIG (water contact angle > 110°) can effectively prevent BxHyIG from being eroded and swollen by water, thereby achieving reliable underwater sensing. More importantly, by directly exposing BxHyIG to air or storing it in nitrogen, the surface adhesion of conductive ionogels can be effectively regulated to obtain double-sided, single-sided or even nonadhesive ionogels. Therefore, this study provides new ideas for the development of conductive ionogels that can be applied under various environmental conditions.

A Stochastic FRET Study on the Core Dimension of Polystyrene-block-Poly(Polyethylene Glycol Monomethyl Ether Acrylate) Micelles.

Polystyrene-b-poly(polyethylene glycol monomethyl ether acrylate) (PSt-b-PPEGA) copolymers featuring pyrene and perylene as the Förster resonance energy transfer (FRET) donor (denoted as D-BCP) and acceptor (denoted as A-BCP), respectively, were synthesized via the reversible addition and fragmentation chain transfer (RAFT) polymerization. These copolymers were then used to form DA-mixed micelles via a dialysis method. The micelles consisted of D-BCP (mole fraction fD = 0.04), A-BCP (fA = 0.04), and label-free PSt-b-PPEGA (fN = 0.92). The decrease in fluorescence intensity of pyrene in the micelles confirmed the occurrence of FRET, with an observed efficiency of 0.32. A Monte Carlo approach was employed to estimate the expected FRET efficiency, assuming the random fractional distribution of D-BCP and A-BCP, along with the random spatial distribution of pyrene and perylene within the micellar core. The observed FRET efficiency suggested a core radius (Rc) of 0.95R0, where R0 was the Förster critical distance. With R0 calculated to be 3.2 nm based on Förster theory, Rc was determined to be approximately 3.0 nm, aligning closely with the dried-out core radius estimated from aggregation number and polystyrene density. This stochastic FRET methodology was further applied to investigate the swelling behavior of the polymer micelles in a mixture of N,N-dimethylformamide (DMF) and water. Dynamic light scattering analysis revealed minimal change in core dimension below 60 vol % DMF content. However, FRET analysis provided a deeper insight, showing an increase in core radius with DMF content up to 20 vol %, followed by saturation up to 50 vol %, offering a more comprehensive understanding of the micelle swelling behavior.

Synthesis of Biodegradable Medical Materials Based on Grafted Acrylate Copolymers on Collagen Obtained under Photocatalysis Conditions

Synthesis of Biodegradable Medical Materials Based on Grafted Acrylate Copolymers on Collagen Obtained under Photocatalysis Conditions

Ultra-stable ionogels based on hydrogen networks with broad temperature, environment, and long-term stability

Ionogels with broad temperature, environment, and long-term stability are desirable in intelligent flexible electronics. Herein, we have developed a novel ultra-stable ionogel through hydrogen bonding between the amphiphilic ionic liquid--1-ethyl-3-methylimidazolium bis[(trifluoromethyl)sulfonyl]imide ([EMIM][NTf2]) and butyl acrylate (BA)-ethyl ethoxyethyl acrylate (EO) copolymer (P(BA-co-EO)). The ionogel demonstrates high decomposition voltage, strong adhesion stability, non-corrosive stability, and cyclic strain sensing stability (500 cycles at 120 % strain). Additionally, it exhibits broad temperature and environment adaptability, capable of stretching up to 7 times at −20 °C, maintaining consistent weight after 30 days of storage in extreme environments such as low/high temperatures (−20∼100 °C), high vacuum (6 × 10−4 Pa), and underwater (without additional sealed packaging), while also maintaining electrophysiological monitoring at −20 °C or 100 °C. Most importantly, the ionogel without sealing can self-adhere to the human skin for continuous and high-quality electrophysiological monitoring for 1 month under daily life conditions. We have utilized the ionogel to fabricate an ionic skin with multifunctional sensing capabilities for strain, pressure, and temperature, which has been successfully employed in human motion and pressure detection. It is believed that ionogels with long-term stability will pave the way for developing next-generation intelligent flexible electronics in future research endeavors.

Sensitisation to the acrylate co-polymers glyceryl acrylate/acrylic acid co-polymer, sodium polyacrylate and acrylates/C10-30 alkyl acrylate cross-polymer (Carbopol®) is rare.

Acrylate polymers and cross-polymers (ACPs) are frequently used cosmetic ingredients. The British Society for Cutaneous Allergy (BSCA) and the UK Cosmetic, Toiletry and Perfumery Association (CTPA) collaborated to investigate the allergenic potential of three commonly-used ACPs. The objective of this study is to determine the prevalence of allergic contact dermatitis (ACD) to three ACPs: glyceryl acrylate/acrylic acid co-polymer, sodium polyacrylate, and acrylates/C10-30 alkyl acrylate cross-polymer (Carbopol®). The BSCA prospectively audited data collected from 20 centres in the UK and Ireland between 1st September 2021 and 1st September 2022. Patients with suspected ACD to (meth)acrylates, with facial dermatitis, or consecutive patients, were patch tested to glyceryl acrylate/acrylic acid co-polymer 10% aqueous (aq.) sodium polyacrylate 2% aq., and to acrylates/C10-30 alkyl acrylate cross-polymer 2% aq. (Carbopol®). The frequencies of positive, irritant, and doubtful reactions were recorded. In total, 1302 patients were patch tested. To glyceryl acrylate/acrylic acid co-polymer, there was one doubtful reaction in a patient allergic to multiple (meth)acrylates, and one irritant. To sodium polyacrylate, there were four irritant reactions, one doubtful, and one positive reaction; in all cases, relevance was unknown and there was no demonstrable (meth)acrylate allergy. There were no reactions to Carbopol®. Sensitisation to these concentrations of the three tested ACPs is rare. Elicitation of dermatitis in (meth)acrylate-sensitised patients by exposure to these three ACPs appears unlikely.

Direct Acrylation of Soybean Oil and the Influence of the Acrylation Degree on Waterborne Acrylic Systems.

The direct acrylation of soybean oil was investigated by the activation of soybean oil's (SO's) internal fatty unsaturation with acidic catalysts. The effect of the catalyst and the reactant ratio with respect to the unsaturation and reaction time on the direct acrylation process were explored. ASO (acrylated soybean oil) with acrylation degrees (the number of acrylate molecules introduced in a triglyceride molecule) between 1.6 and 2.55 were obtained. The effect of the ASO acrylation degree on copolymerization processes was investigated. The resulting monomers were successfully copolymerized with meth(acrylate) monomers by the miniemulsion polymerization process, favoring the droplet nucleation mechanism and showing conversions higher than 97%. The acrylic-ASO copolymers presented lower Tg and higher hydrophobicity and oleophobicity than the acrylic copolymer.

Random Copolymers Based on 2-Ethylhexyl Acrylate Exhibit Unusual Glass Transition Breadth and Facile Autonomous Self-Healing over a Broad Composition Range.

Statistical copolymers are commercially important because their properties can be tuned by comonomer selection and composition. Rubbery-state styrene (S)/n-butyl acrylate (nBA) copolymers have previously been reported to exhibit facile, autonomous self-healing over a narrow composition band (47/53 to 53/47 mol%). The need for a narrow composition band is explained by alternating comonomer sequences that accommodate interchain secondary bonding. It is hypothesized that copolymers that achieve interchain secondary bonding without alternating sequences can exhibit facile self-healing over a broad composition range. 2-ethylhexyl acrylate (EHA) is identified as yielding sequence-independent secondary bonding interactions. For these interactions it is tested experimentally by glass transition breadth in rubbery-state S/EHA copolymers, with S/n-hexyl acrylate (nHA) and S/nBA copolymers as controls. The n-alkyl acrylate random copolymers exhibit enhanced glass transition breadths over narrow composition bands that correspond to autonomous self-healing. In contrast, S/EHA copolymers exhibit much greater glass transition breadths than S/nHA and S/nBA copolymers at all compositions tested as well as self-healing of damage over a broad composition range with full tensile-property recovery, often in 3-10h. Characterization of glass transition breadth may serve as a simple screening tool for identifying copolymers that exhibit broad-composition-range, facile, autonomous self-healing and contribute to polymer resilience and sustainability.

Synthesis of acrylate copolymer‐based super oil adsorption resins and their performances

AbstractIn this paper, an acrylate copolymer‐based oil adsorption resin was designed and synthesized by a suspension polymerization with octadecyl acrylate (SA) and butyl acrylate (BA) as monomers, divinylbenzene (DVB) as a cross‐linking agent, and toluene as a pore‐forming agent. By studying the synthesis conditions, the copolymer “SA‐BA‐DVB” (PSBA) with the best adsorption capacity was obtained, when the molar ratio between SA and BA was about 0.9, the content of the DVB and PVA 1788 was about 0.107 wt% and 1.0 wt%, respectively, accounting for the total mass amount of the monomers. Furthermore, by introducing 2% reactive silica nanoparticles (R‐SiO2), the performances of the PSBA were improved due to its increased hydrophobicity and activity space. The equilibrium adsorption capacity of the resulted R‐SiO2/PSBA to kerosene, diesel oil, benzene, and p‐xylene was 31.90, 34.13, 39.44, and 41.81 mL/g, respectively, which is about 1.12 to 1.21 times higher than that of the PSBA. Also, the R‐SiO2/PSBA show brilliant oil retention rate of about 99% after centrifugation at 3000 rpm for 5 min and recycling ability which can be reusable for at least 10 absorption‐desorption cycles without capacity change, demonstrating that the obtained R‐SiO2/PSBA resin can be used as oil removing agents in the field of oil spill applications.Highlights R‐SiO2 modified acrylate copolymer as an oil adsorption resin was designed and synthesized. The influence of the monomers, cross‐linking agent, and others on the adsorption resin was systematically studied. The adsorption kinetics and performances of the adsorption resin were studied.

Acrylate-Based PEG Hydrogels with Ultrafast Biodegradability for 3D Cell Culture.

Poly(ethylene glycol) (PEG)-based hydrogels are particularly challenging to degrade, which hinders efficient cell harvesting within the gel matrix. Here, highly branched copolymers of PEG methyl ether acrylate (PEGMA) and disulfide diacrylate (DSDA) (PEG-DS) with short primary chains and multiple pendent vinyl groups were synthesized by a "vinyl oligomer combination" approach. PEG-DS readily cross-links with thiolated gelatin (Gel-SH) to form hydrogels. Results demonstrate that shortening the primary chains of PEG-DS significantly enhances the viability of bone marrow mesenchymal stem cells (BMSCs) by up to 193.2%. Importantly, DS junctions can be easily cleaved into short primary chains using dithiothreitol (DTT), triggering ultrafast degradation of PEG-DS/Gel-SH hydrogels within 2 min under mild conditions and release of the encapsulated BMSCs. This study establishes a novel strategy to enhance the degradation of acrylate-based PEG hydrogels for three-dimensional (3D) cell culture and harvesting. These findings expand the potential applications of such hydrogels in various biomedical fields.