Latex Particles Research Articles

Characterisation of particle single-scattering albedo with a modified airborne dual-wavelength CAPS monitor

Abstract. Atmospheric aerosols impact the Earth's climate system directly by scattering and absorbing solar radiation, and it is important to characterise the aerosol optical properties in detail. This study reports the development and validation of an airborne dual-wavelength cavity-attenuated phase-shift (CAPS) single monitor, named A2S2 (Aerosol Absorption Spectral Sizer), based on the commercial CAPS single-scattering albedo monitor (CAPS-PMSSA; Aerodyne), to simultaneously measure the aerosol optical scattering and extinction at both 450 and 630 nm wavelengths. Replaced pressure and temperature sensors and an additional flow control system were incorporated into the A2S2 for its utilisation on board research aircraft measuring within the troposphere. The evaluation of A2S2 characteristics was performed in the laboratory and included the investigation of the signal-to-noise ratio, validation of performance at various pressure levels, optical closure studies and intercomparing with the currently validated techniques. The chamber experiments show that the A2S2 can perform measurements at sample pressures as low as 550 hPa and at sample temperatures as high as 315 K. Based on the Allan analysis results, we have evaluated that the minimum detection limit of the measurements shows that the measurements have a limit accuracy of ∼ 2 Mm−1 at 450 nm and ∼ 1 Mm−1 at 630 nm for 1 Hz measurements of both scattering coefficients (σsca) and extinction coefficients (σext). The optical closure study with size-selected polystyrene latex (PSL) particles shows that the truncation error of the A2S2 is negligible for particles with particle volume diameter (Dp) < 200 nm, while, for the larger sub-micrometre particles, the measurement uncertainty of A2S2 increases but remains less than 20 %. The average factors to correct the truncation error are 1.13 and 1.05 for 450 and 630 nm, respectively. A simplified truncation correction, dependent on the scattering Ångström exponent (SAE), was developed to rectify truncation errors of the future A2S2 field measurement data. The σsca and σext measured by the A2S2 show good agreement with the concurrent measured results from the nephelometer and the CAPS particle extinction monitor (CAPS-PMex). The absorption coefficient (σabs) derived through the extinction-minus-scattering (EMS) method by the A2S2 also corresponds with the results obtained from the aethalometer. The A2S2 was successfully deployed during an aircraft measurement campaign (Atmospheric ChemistRy Of the Suburban foreSt – ACROSS) conducted in the vicinity of Paris and the surrounding regions. The average SSA measured during the entire ACROSS flight campaign is 0.86 and 0.88 at 450 and 630 nm, respectively, suggesting that light-absorbing organic aerosols play a significant role. The average SAE and absorption Ångström exponent (AAE) varied due to measurements in various pollution conditions. The results presented in this study indicate that the A2S2 instrument is reliable for measuring aerosol σsca and σext at both blue and red wavelengths, and it stands as a viable substitute for future airborne evaluations of aerosol optical properties.

Broad-Spectrum Supramolecularly Reloadable Antimicrobial Coatings.

Antimicrobial surfaces limit the spread of infectious diseases. To date, there is no antimicrobial coating that has widespread use because of short-lived and limited spectrum efficacy, poor resistance to organic material, and/or cost. Here, we present a paint based on waterborne latex particles that is supramolecularly associated with quaternary ammonium compounds (QACs). The optimal supramolecular pairing was first determined by immobilizing selected ions on self-assembled monolayers exposing different groups. The QAC surface loading density was then increased by using polymer brushes. These concepts were adopted to develop inexpensive paints to be applied on many different surfaces. The paint could be employed for healthcare and food production applications. Its slow release of QAC allows for long-lasting antimicrobial action, even in the presence of organic material. Its efficacy lasts for more than 90 washes, and importantly, once lost, it can readily be restored by spraying an aqueous solution of the QAC. We mainly tested cetyltrimethylammonium as QAC as it is already used in consumer care products. Our antimicrobial paint is broad spectrum as it showed excellent antimicrobial efficiency against four bacteria and four viruses.

Crosslinking using particulate crosslinker in polymer latex film-coating process for controlled-release fertilizer

Fertilizing controlled-release fertilizer is apt to keep a reasonable concentration of nutrient in soil and increase the efficiency of fertilizer utilization. The production of film-coated controlled-release fertilizer using polymer latex is a green process. However, the release period is usually short because the film crosslinking density is low during the fast film formation of the dynamic granule coating. In this study, numerous epoxy groups were grafted onto the nanoparticle surface of single-particle-dispersed silica to prepare particulate crosslinker with abundant crosslinking sites. The epoxy groups on the surface of the particulate crosslinker reacted with the carboxyl groups on the surface of the styrene-acrylate latex particles during film formation, enhancing film crosslinking. With the addition of the particulate crosslinker, the polymer latex was used to coat urea granules in a fluidized bed via spray coating at a low coating content of 4 wt%. The release period of film-coated urea granules with an enhanced crosslinking film reached 40 d, which was five times longer than that in the absence of particulate crosslinker.

Preparation of organosilicon and organofluorine synergistically modified amphiphilic branched polyurethanes and their application in diisocyanate emulsifiers

AbstractIsocyanate‐based monomers and polymers have found widespread industrial application; however, the realization of green water‐based products via the preparation of stable isocyanate aqueous emulsions remains challenging. Herein, a series of organosilicon and organofluorine synergistically modified amphiphilic branched polyurethanes (HBWPU), synthesized by grafting perfluorohexyl ethanol semi‐terminated isophorone diisocyanate (IPDI) onto a hydrophilic polyurethane prepolymer, is presented. Subsequently, using a physical mixing method, stable diisocyanate emulsions are fabricated by preparing diisocyanate latex particles with IPDI as the core and hyperbranched water‐based polyurethanes (HBWPU) as the shell. Structural investigations showed that the branching degree and fluorine content of the HBWPU significantly affects the stability of the diisocyanate emulsions. Increasing the degree of branching from 0.34 to 0.86 causes the amount of residual isocyanate (NCO) groups to decrease from 20.1% to 16.7%. In contrast, an increase in the fluorine content from 0% to 17.8% increases the amount of residual NCO groups from 11.5% to 24.6%. Thus, HBWPU can be used as an emulsifier to prepare waterborne diisocyanate cross‐linking agents. Such polyurethane‐coated isocyanate aqueous emulsions can increase the hardness and significantly improve the acetone resistance of hydroxyl polyacrylate resins.

Fabrication of core-shell polyacrylate latex pressure sensitive adhesives modified by fluorinated monomer and film properties

In this work, a series of fluorinated core-shell polyacrylate latex pressure sensitive adhesives (PSAs) were successfully synthesized through monomer-starved seeded semi-continuous emulsion polymerization. Specifically, (meth)acrylate monomers were employed as the main materials, with dodecafluoroheptyl methacrylate (DFMA) were used as modified monomer. The impact of fluorine monomer DFMA on the resulting core-shell latex and PSA properties was thoroughly examined. FTIR analysis confirmed the successful incorporation of DFMA into the latex copolymer through emulsion polymerization. TEM images illustrated that the morphology of latex particles exhibit a distinct core-shell structure. The results also showed that with the addition of DFMA, the water absorption and water whitening of the latex films decreased, while the water contact angle and thermal stability are improved. Interestingly, the latex films with DFMA added to the shell phase exhibit a larger WCA value when compared to those with DFMA in the core phase, further confirmed by XPS results. Finally, the adhesive properties of the fluorinated core-shell acrylate PSA were evaluated. The results of shear strength and gel content demonstrate that the prepared PSA exhibits excellent cohesive properties. Thus, this work could present a feasible strategy for optimizing the comprehensive properties of acrylate latex PSAs.

Preparation and application of the water‐based acrylic self‐polishing resin: Good storage stability, good film‐forming matrix of marine antifouling coatings

AbstractIn order to reduce the release of volatile organic compounds (VOCs), it is of great practical significance to develop water‐based self‐polishing antifouling coatings instead of traditional acrylic self‐polishing antifouling coatings. However, when preparing film forming matrix resin emulsions for water‐based antifouling coatings, the use of emulsifiers in large amounts causes film‐forming defects and poor adhesion. Herein, soap‐free emulsion polymerization is utilized to prepare resin emulsions by copolymerization of hydrophilic monomers, lipophilic monomers and polymerizable hydrophilic ionic monomers. The hydrophilic structure can give the water‐based polymer self‐emulsification function to maintain the stability of the emulsion and can promote the fusion between the latex particles by forming hydrogen bonds and coordination bonds, and its connection with the pigments and fillers in the coating can also promote the excellent film formation of the coating. The experimental results show that the water‐based self‐polishing antifouling resin emulsion has good storage stability and compatibility with the pigments and fillers. The coatings formulated using this emulsion as the film‐forming matrix firmly adhered to substrates and displayed satisfactory antifouling performance even after being exposed to a real sea environment for 18 months. This study presents a simple approach for the development of water‐based resin emulsion with good storage stability and good water‐based self‐polishing marine antifouling coatings.

Synthesis of Latex Particles with Biomolecules on the Surfaces by RAFT Emulsion Polymerization and Surface Biomineralization

Synthesis of Latex Particles with Biomolecules on the Surfaces by RAFT Emulsion Polymerization and Surface Biomineralization

Improving the adhesion strength and moisture resistance of poly(vinyl acetate) latex as wood adhesive via blending with gelatin

Gelatin can act as wood adhesive for fabrication of numerous structures. Polyvinyl acetate (PVAc) is also used as wood adhesive because it provides excellent adhesion. Unfortunately, its bonds are sensitive to humid atmospheres especially at elevated temperatures. The current work explores hybridization of PVAc emulsion with finite amounts of gelatin and the resulting latex was fully characterized using different techniques, where it was found that gelatin insertion caused densification of the latex structure without affecting its stability while the viscosity increased without visual phase separation, indicating strong interactions emerged between both. Dynamic light scattering (DLS) and transmission electron microscope (TEM) confirmed a mean size of the latex particles increasing from 265 nm to 290 nm in presence of elevated doses of gelatin, with the surface charge decreasing from −42 mV to −33 mV. Turbidity measurements revealed the latex particles became more likely to coagulate in presence of increasing amounts of gelatin and formation of a more compact film that provides higher resistance to water permeation and stronger adhesion as supported by shear strength evaluations. Differential scanning calorimetry (DSC) and thermogravimetric analysis (TGA) proved strong interactions between PVAc with gelatin, causing higher thermal stability and possibility of use at relatively higher temperatures. X-ray diffraction (XRD) showed broadening of the peak at 2θ = 21° indicating partial destruction of the triple helical structure of gelatin, which can be correlated with the spectra of Fourier transform infrared (FTIR) that showed obvious shifts of the main peaks of PVAc due to effective insertion of gelatin.

Solution of the inverse problem of estimating particle size distributions

In this work, we describe two alternative methods for solving the ill-conditioned inverse problem that allows estimating the particle size distribution (PSD) from turbidimetry measurements. The first method uses the inverse Penrose matrix to solve the inverse problem in its discrete form. The second method consists of replacing an ill-posed problem with a collection of well-posed problems, penalizing the norm of the solution, and it is known as the Tikhonov regularization. Both methods are used to solve a synthetic application of the inverse problem by solving the direct problem using a theoretical expression of the distribution of particles sizes function f(D) and considering soft industrial latex particles (NBR), with average particle diameters of: 80.4, 82.8, 83.6, and 84.5 nm; and three illumination wavelengths in the UV-Vis region: 300, 450, and 600 nm. The estimated solution obtained by the inverse Penrose matrix is different from the original solution due to the inverse problem is ill-conditioned. In contrast, when using Tikhonov’s regularization, the estimate obtained is close to the original solution, which proves that the particle size distribution is adequate.

Cellulose nanocrystals/fluorinated polyacrylate with mechanical tunability, water-oil resistance and self-healing capability via light actuated reversible associations

Traditional fluorinated polyacrylate has been extensively applied in various fields, which is favored by many researchers. However, the polymer usually can lose usefulness when it is damaged. Endowing the polymer with self-healing capability provides a potential solution to address the conflict. Herein, a series of photo actuated self-healing fluorinated polyacrylate based on coumarin groups was synthesized by reversible addition-fragmentation chain transfer (RAFT)-assisted Pickering emulsion polymerization using the modified cellulose nanocrystals as the stabilizer, n-butyl acrylate (BA) as the soft monomer, and methyl methacrylate (MMA) as the hard monomer. The influences of the dosage of 7-(4-vinylbenzyloxy)−4-methylcoumarin) (VBMC) and the mass ratio of BA to MMA on the emulsion polymerization and latex film properties were studied. The results showed that the latex particle size and its distribution decreased and then increased as the VBMC dosage and the mass ratio of BA to MMA increased. The latex film exhibited not only high ultimate tensile stress (6.36 MPa) and large stretchability (575.71%) but also a certain anti-fatigue characteristic. The water and oil contact angles of latex film could reach 118.5° and 101.7°, respectively. Besides, the latex film could achieve efficient self-healing capability due to the mobility of polymer chains associated with low glass transition temperature (Tg) and the reversible [2+2] cleavage/dimerization reaction of the coumarin groups upon ultraviolet (UV) irradiation of 254 nm and 365 nm. The work offers a substantial reference for developing different light actuated self-healing polymers with great prospects and promising futures.

High solid content waterborne polyurethane with high foaming rate to artificial leather: Synthesis and characterization

A type of high solid content waterborne polyurethane (HSWPU) dispersions applied to foamed artificial leathers were designed and prepared by prepolymer method. The solid content of the waterborne polyurethane dispersions could reach 53 %, and the foaming ratio could reach an astonishing 2.50 by adjusting the parameters. The influence of synthesis parameters, including R value (molar ratio of -NCO/-OH), D value (hydrophilic group content), trimethylol propane (TMP) content (degree of crosslinking) and ethylenediamine (EDA) content (it was chain extender) on foaming ratio were investigated. Meanwhile, a series of properties of HSWPU dispersions, films and foamed artificial leathers were introduced in detail. The results demonstrated that R value, TMP content, D value and EDA content synergistically decided the foaming properties of HSWPU dispersions in three aspects: three-dimensional structure, surface tension and polarity, respectively. With optimized parameters of R = 2.0, TMP = 0.4 wt%, DMPA = 3.0 wt% and EDA = 60 wt%, the HSWPU dispersions had good appearance and stability, and the latex particles exhibited excellent water, acid and alkali resistance after films formation. The HSWPU dispersions with high foaming rate without collapsing in the foam-forming process and created uniformly bubble pores. In terms of application properties, the prepared foamed artificial leathers showed admirable air permeability and water vapor transmissions. All results distinctly demonstrate a feasible yet promising paradigm for applying the HSWPU on foamed artificial leathers had great potential applications.

Influence of Eu3+ Doping on Physiochemical Properties and Neuroprotective Potential of Polyacrylic Acid Functionalized Cerium Oxide Nanoparticles.

Cerium oxide nanoparticles (CeONPs) exhibiting antioxidant properties are investigated as potential tools for neurodegenerative diseases. Here, we synthesized polyacrylic acid conjugated cerium oxide (CeO) nanoparticles, and further to enhance their neuroprotective effect, Eu3+ was substituted at different concentrations (5, 10, 15 and 20 mol%) to the CeO, which can also impart fluorescence to the system. CeONPs and Eu-CeONPs in the size range of 15-30 nm were stable at room temperature. The X-ray Photoelectron Spectroscopy (XPS) analysis revealed the chemical state of Eu and Ce components, and we could conclude that all Eu3+ detected on the surface is well integrated into the cerium oxide lattice. The emission spectrum of Eu-CeO arising from the 7F0 → 5D1 MD and 7F0 → 5D2 transitions indicated the Eu3+ ion acting as a luminescence center. The fluorescence of Eu-CeONPs was visualized by depositing them at the surface of positively charged latex particles. The developed nanoparticles were safe for human neuronal-like cells. Compared with CeONPs, Eu-CeONPs at all concentrations exhibited enhanced neuroprotection against 6-OHDA, while the protection trend of Eu-CeO was similar to that of CeO against H2O2 in SH-SY5Y cells. Hence, the developed Eu-CeONPs could be further investigated as a potential theranostic probe.

Влияние дидрогестерона на окситоцинореактивность нейтрофилов венозной крови беременных женщин и родильниц

The ability of steroid hormones to modulate the binding of oxytocin to oxytocin receptors is of great interest. The purpose of this article was to study the effect of oxytocin, dydrogesterone and their mixture on the radical activity of venous blood neutrophils in pregnant women during the 3rd trimester of a normal pregnancy and in women on the 1st day after term delivery. Materials and methods. Using the chemiluminescent method (BChL-07 biochemiluminometer) and cell stimulation with latex particles, we studied non-genomic and genomic effects of dydrogesterone (5∙10–5 g/l), oxytocin (10–7 IU/l) and their mixture on the radical activity of venous blood neutrophils in 20 pregnant women in the 3rd trimester of a normal pregnancy and 10 women on the 1st day after term labour. When the noise level was automatically subtracted, the following were recorded: maximum intensity of the synthesis of reactive oxygen species, time to reach the maximum of synthesis intensity, and area under the chemiluminogram curve, reflecting the total synthesis of radical particles over the course of 30 min. Results. Baseline radical activity of neutrophils in women on the 1st day after term delivery was found to be three times higher than in women during the 3rd trimester of a normal pregnancy. Judging by the area under the chemiluminogram curve and maximum intensity of the synthesis of reactive oxygen species, oxytocin had an equal stimulating effect on venous blood neutrophils both in pregnant women during the 3rd trimester and in puerperae. Dydrogesterone in each group of women equally stimulated the radical activity of neutrophils, both non-genomically and genomically. In both groups, under the action of dydrogesterone through membrane receptors, oxytocin reactivity of neutrophils remained unchanged, while through nuclear receptors, it decreased. Possible mechanisms of progesterone’s involvement in the regulation of oxytocin reactivity of the myometrium and venous blood neutrophils in women during pregnancy and postpartum are considered.

Experimental Study on Modification of Grouting Material for Joints of Prefabricated Buildings

In order to apply grouting material to the joints of fabricated buildings and make it meet the performance demands of low shrinkage, strong bond, and high toughness of joint materials for prefabricated buildings, the expansion agent (EA), neoprene latex (NL), and rubber particles (RP) were used to modify the grouting material, and the effects of different dosages of the three components on the working performance, mechanical properties, and expansion or shrinkage properties of the grouting material were investigated. The results show that the EA decreases the flexural strength-to-compressive strength ratio (FCR) of the grouting material and enhances the vertical expansion rate and bond strength. The dosage of EA and the curing conditions have a significant effect on the expansion rate of the hardened grouting material. The grouting material can still maintain its 0.0022% free expansion rate with a 7% EA dosage at 120 d. The NL significantly inhibits the vertical expansion of the fresh mortar but inhibits the drying shrinkage of the grouting material after hardening, improves the FCR and bond strength; the 7 d bond strength under a 5% NL dosage can reach 4.27 MPa. The RP inhibits the vertical expansion of the fresh mortar and the drying shrinkage after mortar hardening; with the increase of its dosage, the bond strength of the grouting material increases first and then decreases, the 28 d FCS of the grouting material peaked at 0.173 at 10% dosage.

The Relationship between Serum Zonulin and Innate Immunity in Patients with Inflammatory Bowel Disease

The aim of the study was to investigate the relationship between the serum zonulin and the cellular immunity in patients with ulcerative colitis (UC) and Crohn’s disease (CD). The study included 97 patients, 13 (13.4%) patients with CD and 84 (86.6%) patients with UC. The concentration of zonulin in the serum was studied using the ELISA kits. The investigation of the circulated leukocyte subpopulation was carried out through flow cytometry. The functional activity of the circulating neutrophils was studied using the absorption capacity of the monodisperse polystyrene latex particles and indicators of oxygen-dependent metabolism in the nitroblue tetrazolium test. The serum zonulin concentration in CD patients was significantly higher compared with UC patients (p = 0.003). The zonulin concentration directly correlated with the functional activity of the circulating neutrophils. Patients with a zonulin concentration > 472.4 pg/mL had a significantly higher number of band neutrophils (p = 0.0104), CD3+CD8+ cells (p = 0.0212), NK cells (p = 0.0161), and lower–CD19+ cells (p = 0.0034). Among the IBD patients, zonulin was associated with IBD severity. An increase in the serum concentration of zonulin was associated with an increase in the functional activity of circulating neutrophils and an increase in the number of CD3+CD8+ cells, NK cells, and a decrease in the number of CD19+ cells.

Preparation of light‐responsive block copolymer modified cellulose nanocrystal@polydopamine particle and its application in fluorinated polyacrylate film

AbstractLight‐responsive cellulose nanocrystal@polydopamine (CNC@PDA) modified fluorinated polyacrylate was synthesized by Pickering emulsion polymerization with light‐responsive block copolymer modified CNC@PDA as stabilizer. The epoxy groups in poly(acrylic acid‐co‐acrylamide)‐b‐poly(glycidyl methacrylate)‐b‐poly(hexafluorobutyl acrylate‐co‐coumarin) amphiphilic triblock copolymer reacted with the hydroxyl and amino groups on the surface of CNC@PDA to form the modified CNC@PDA. The successful preparation of modified CNC@PDA was confirmed by means of FT‐IR, XRD, TG, UV–Vis, surface tension measurement, and X‐ray photoelectron spectroscopy (XPS) techniques. The results showed that the modified CNC@PDA had light‐responsive and amphiphilic properties, and could be used as stabilizer to form stable Pickering emulsion. And the influence of modified CNC@PDA dosage on emulsion polymerization and film performance was systematically studied. The latex particle size decreased initially with increasing modified CNC@PDA dosage, from 0.6 to 1.0 wt%, and then increased. The mechanical, self‐healing, and water–oil repellent properties of film were enhanced initially with increasing modified CNC@PDA dosage, from 0.6 to 1.0 wt%, and then declined. Atomic force microscope confirmed that the latex film had a rough surface. Moreover, the latex film comprising 1.0 wt% modified CNC@PDA presented not only high tensile strength (4.92 MPa), large elongation at break (657.70%), and superior oil/water repellency but also excellent self‐healing property.

Electrical detachment of bumpy particles and rough spherical particles charged by corona ions

ABSTRACT Electrostatic detachment of bumpy and spherical particles with rough surfaces charged by corona ions was studied. Corona charging leads to uniformly distributed charges across the entire particle surface. The JKR adhesion model and electrostatic interactions of these particles in contact with a surface were evaluated. The electrostatic forces for particles carrying fixed charges per unit mass were evaluated. The study investigated the electric fields required to detach charged particles from rough surfaces for different charge levels, various numbers of bumps for bumpy particles, and different numbers of contact asperities for rough spherical particles. The accuracy of the model predictions for detaching charged particles from substrates with varying degrees of roughness was assessed by comparison with the experimental data, which indicated that the predicted electric detachment fields agreed with the experimental data for the selected range of parameters. The proposed model provides a helpful framework for removing bumpy particles, and rough spherical particles charged by corona ions in various applications. For 8.3 μm polystyrene charged latex particles, approximately 46% and 62% reductions in detachment electric field were found for a 10% decrease in the roughness parameter for bumpy particles and rough spheres, respectively.

Polymer Versus Polymerization Fouling: Basic Deposition Mechanisms During Emulsion Polymerization by the Example of a Vinyl Acetate and Versa 10 Copolymer

AbstractThe deposition process during emulsion polymerization can be classified as both particulate and reaction fouling, but a deeper understanding of the deposition mechanism, especially in combination with the polymerization process, is lacking. Here, a more in‐depth understanding of the deposition mechanism is sought by investigating the fouling formation of a Vinyl acetate and Versa 10 copolymer on a heated stainless steel surface during emulsion polymerization. Its deposition behavior is also compared with the behavior of an already reacted polymer. All possible influencing factors are investigated separately, and the fouling is quantified by the mass based fouling resistance and the fouling layer composition. The fouling rates of both experimental approaches (ongoing reaction versus already reacted polymer) are used to determine the fraction of reaction fouling along the reaction pathway. The solids content and the driving temperature difference are identified as the main factors influencing fouling formation. The deposited material is composed of latex particles and emulsifier with particle size and number depending on the respective equilibrium composition of the fluid phase. The reaction fouling rate is correlated with the proportion of free initiator radicals and the amount of dissolved monomer in the aqueous phase.

Enhancing formation and retention of hollow structural integrity through intermediate and outermost layer design in seeded emulsion polymerization of hollow latex particles

AbstractThe synthesis of hollow latex particles through seeded emulsion polymerization involves a series of intricate steps, including the formation of distinct polymer layers with specific properties. Despite extensive research, preserving the desired hollow structure remains challenging due to the unclear role of the encapsulating polymer layers. This study systematically adjusts the glass transition temperature (Tg) of the intermediate layer by varying the butyl acrylate (BA) ratio in the monomer feed mixture. By controlling the reaction temperature during alkali swelling, we explore the critical influence of Tg on hollow latex particle formation from carboxylated core latex particles. To ensure long‐term hollow structure retention after drying, a rigid outer layer is polymerized onto the intermediate layer. Surprisingly, higher divinylbenzene (DVB) mass ratios (5.0 and 10.0 wt%) do not result in a highly crosslinked hollow shell due to DVB self‐nucleation. This paper emphasizes the importance of precise design parameters for both intermediate and outermost layers in achieving and maintaining hollow latex particle structures. Understanding each layer's role and optimizing their compositions contribute to advancing hollow latex particle synthesis through seeded emulsion polymerization.

Enhanced Stability and Catalytic Activity of a Nanocatalyst with Reusable Ionic Liquid Hydrogels for the Reduction of Organic Pollutants.

Nitroaromatic compounds have a wide range of applications. However, they pose a significant threat to both the environment and human health. Ionic liquid hydrogels (ILs-gels) have emerged as a cost-effective and environmentally friendly option for various applications. However, conventional ILs-gels are known to possess mechanical flaws or defects. The procedure utilized a facile synthesis route that involved the polymerization of acrylamide (AM) and ionic liquids (ILs) to create a novel candidate for nanoparticle absorption. This study resolved this issue by creating toughened hydrophobic combined hydrogels synthesized through the addition of SiO2@poly(butyl acrylate) core-shell inorganic-organic hybrid latex particles (SiO2@PBA) to the AM-ILs mixture. The SiO2@PBA particles were chosen to provide the hydrogels with exceptional stretchability (up to 4050% strain) and high mechanical properties (tensile strength of 126 kPa) by acting as both a nanotoughener and a cross-linking point for hydrophobic linkage. Additionally, the P(AM/ILs)-SiO2@PBA hydrogel served as a template for the in situ and stable formation of palladium (Pd) nanoparticles. By incorporation of these Pd nanoparticles as catalysts into P(AM/ILs)-SiO2@PBA hydrogel carriers, the resulting P(AM/ILs)-SiO2@PBA/Pd hydrogels exhibited the ability to catalyze the degradation of p-nitrophenol. Remarkably, even after 15 applications, the efficiency of the degradation process remained consistently above 90%. Thus, the innovative SiO2@PBA toughened ILs-hydrogel design strategy can be utilized to develop robust and stretchable hydrogel materials for catalytic use in the sewage disposal industry.