Butyl Acrylate Research Articles

Cerium Oxide‐Armored Composite Latex Particles by Visible Light Emulsion Photopolymerization: From Synthesis to Film Properties

AbstractCerium dioxide (CeO2) has huge potential in many applications ranging from biochemical engineering to the coating industry. Here, the first example of visible light photo‐mediated Pickering emulsion polymerization of (meth)acrylate monomers is reported using CeO2 nanoparticles (NPs) as solid stabilizer. A ω,ω′−dicarboxylic acid diphenyl disulfide photoinitiator is anchored on the surface of the CeO2 NPs and used to initiate the emulsion polymerization of methyl methacrylate (MMA) and of MMA/n‐butyl acrylate (MMA/BA) under visible light leading to CeO2‐armored latexes. Radicals generated upon light irradiation trigger the formation of polymer chains chemically attached to the CeO2 NPs, promoting their subsequent adsorption on the latex surface. The composite films obtained from the CeO2‐armored P(MMA‐co‐BA) latexes exhibit a unique honeycomb nanostructure with the nanoceria located in the walls giving the materials excellent mechanical, anti‐UV, and photocatalytic properties.

Effect of Hydrophobic Acrylic Monomers with Different Alkyl Side Chain Lengths on Reducing the Glistening of Hydrophobic Acrylic Intraocular Lens Materials

AbstractGlistening is the condensation of water that forms within the intraocular lens (IOL) materials. In this study, a new approach was attempted to reduce the glistening of IOL materials by introducing hydrophobic acrylic monomers with different alkyl side chain lengths into the IOL materials. Various hydrophobic acrylic monomers such as butyl acrylate (BA), 2‐ethylhexyl acrylate (EHA), and dodecyl acrylate (DA) were copolymerized with a hydrophobic acrylic monomer, 2‐phenoxyethyl acrylate, respectively. In this process, we investigated the effect of the alkyl side chain lengths of hydrophobic acrylic monomers on the glistening of hydrophobic acrylic IOL materials. As the content of hydrophobic acrylic monomers (BA, EHA, and DA) increased, the glistening of IOL materials decreased significantly for all hydrophobic acrylic monomers. At the same content of hydrophobic acrylic monomers, the IOL material showed the least content of glistening when copolymerized with DA. However, the IOL material obtained using BA exhibited the largest content of glistening, indicating that the glistening reduction effect was large in the order of DA>EHA>BA. These findings show that the glistening of IOL materials decreases with increasing alkyl side chain lengths of hydrophobic acrylic monomers.

Preparation of low‐temperature self‐crosslinking acrylic resin and its performance research

AbstractAcrylic resin, as a common coating and adhesive, possesses excellent heat resistance, weather resistance, and is inexpensive, making it widely used in industries related to automotive, construction, electronics, fabrics, and other sectors essential to our daily life. Traditional acrylic resin not only pollutes the environment but also poses certain health risks. Therefore, we studied the synthesis of a low‐temperature self‐crosslinking acrylic emulsions were synthesized by free radical solution polymerization using methyl methacrylate (MMA), butyl acrylate (BA), acrylic acid (AA), diacetone acrylamide (DAAM), hydroxypropyl acrylate (HPA), epoxy resin (E‐51) as the monomers, vinyltriethoxysilane (A‐51) as the coupling agent, and adipic dihydrazide (ADH) as the cross‐linking agent. This water‐based acrylic resin undergoes a crosslinking reaction between the carbonyl group of DAAM and the hydrazide group of ADH, substantially improved the drying speed and adhesion compared to unmodified versions, and also improved the thermal stability. The contact angle of the film increased from 72.8° to 86.9° with the increase of the degree of cross‐linking, and the mechanical properties were improved by 60%. This study provides a suitable formulation for preparing water‐based acrylic resins with superior performance.

Multi-Responsive Polymer Nanoparticles: A Versatile Platform for Double-Security Anticounterfeiting and Smart Food Packaging.

Potential applications of colloidal polymer nanoparticles in the preparation of smart inks are investigated by physical incorporation of the oxazolidine molecules. Precise adjusting the polymer chain flexibility and polarity is achieved by controlling the ratio of methyl methacrylate and butyl acrylate monomers in the polymerization reaction. In addition, nanofibrous indicators of acid-base vapors are prepared from the latex nanoparticles. This can be beneficial for creating materials that sense and respond to environmental changes, such as humidity or moisture and acidity. Thermochromic inks are prepared by microencapsulating crystal violet lactone dye (CVL) in polymer matrices to prevent their release into the aqueous media. Combining two distinct systems with varying triggers, such as light and temperature, provides an effective strategy for double-encryption anticounterfeiting and crack and scratch detection and indication applications. Preparing labels impregnated with double-responsive inks, a novel approach is developed for food spoilage detection and preservation indication. Labels are manufactured using polymer nanoparticles, which contain photoluminescent oxazolidine molecules, as well as a trinary mixture of CVL within core-shell latex particles as the thermochromic dye. The combination of these two responsive elements transforms traditional packaging into a dynamic and interactive sentinel for the food it holds.

Development of cellulose-supported Pd-nanocatalyst for the heck coupling and michael addition reactions

The development of reusable, bio-resource based nanocatalysts with high turnover numbers (TONs) is essential for increased sustainability in the chemical sector. Herein, cellulose-supported bio-resourced poly(hydroxamic acid) is employed as a ligand in the synthesis of a palladium nanocomposite (PdNc-PHA) that exhibits higher TONs that previously reported similar systems for the Mizoroki-Heck and Michael addition reactions. The PdNc-PHA catalyst was characterised using Fourier transform infrared spectroscopy (FTIR), field-emission scanning electron microscopy (FE-SEM), energy dispersive X-ray spectrometry (EDX), high-resolution transmission electron microscopy (HR-TEM), X-ray photoelectron spectroscopy (XPS), and inductively coupled plasma-atomic emission spectroscopy (ICP-AES) analyses. Results showed that the PdNc-PHA catalyst exhibits excellent durability and high catalytic activity in the Mizoroki-Heck and Michael addition reactions, leading to high yields of the desired corresponding products. The Mizoroki-Heck reaction of aryl/heteroaryl chlorides with olefins resulted in the production of cross-coupled products, while the Michael addition reaction of phenol/thiophenol and aliphatic cyclic/alicyclic amines with a variety of olefins synthesised the corresponding O-, S-, and N-alkylated products. The recycle and reusability of the catalyst were tested using 4-nitrochlorobenzene and butyl acrylate. The results demonstrated that the catalyst maintained its catalytic activity effectively for up to ten cycles without any noticeable loss in performance. This research represents a promising strategy for efficient catalysis based on bio-waste as a wealth material.

Synthesis and properties of superhydrophobic monomer stearyl methacrylate-modified polyacrylate latex pressure sensitive adhesives

Hybrid surfactants of long carbon chain hydrophobic nonionic emulsifier N-390 and conventional anionic emulsifier CO-436 were utilized in this study to enable successful emulsion polymerization of super-hydrophobic monomer stearyl methacrylate (SMA) together with butyl acrylate (BA), acrylic acid (AA), and 2-hydroxyethyl acrylate (HEA). The influences of SMA on the resulting latex and film properties were thoroughly investigated. Both FTIR and 1H NMR were used to confirm the successful participation of SMA in the emulsion polymerization. The results indicated that with introduction of SMA, the roughness of the latex film increases, while the light transmission decreases. It was also found that with the addition of SMA, contact angle of the latex PSA film increased from 115.1° to 127.2°, while water absorption decreased from 5.76 to 2.89 wt%. DSC curves demonstrated that SMA has participated more in the homopolymerization reaction than in the copolymerization reaction. TGA results showed that the initial decomposition temperature (T5%) of the latex film was increased from 302.8 to 332.7 °C with the increase of SMA dosage from 0 to 20 wt%. Finally, adhesion properties results indicated that loop tack and 180° peel force of the PSA films were decreased from 11.51 to 1.88 N/25 mm and 6.36 to 3.44 N/25 mm, respectively, while shear strength was increased from 732 to 2865 min.

Interfacial fatigue fracture of pressure sensitive adhesives

Pressure sensitive adhesives (PSAs) are viscoelastic polymers that can form fast and robust adhesion with various adherends under fingertip pressure. The rapidly expanding application domain of PSAs, such as healthcare, wearable electronics, and flexible displays, requires PSAs to sustain prolonged loads throughout their lifetime, calling for fundamental studies on their fatigue behaviors. However, fatigue of PSAs has remained poorly investigated. Here we study interfacial fatigue fracture of PSAs, focusing on the cyclic interfacial crack propagation due to the gradual rupture of noncovalent bonds between a PSA and an adherend. We fabricate a model PSA made of a hysteresis-free poly(butyl acrylate) bulk elastomer dip-coated with a viscoelastic poly(butyl acrylate-co-isobornyl acrylate) sticky surface, both crosslinked by poly(ethylene glycol) diacrylate. We adhere the fabricated PSA to a polyester strip to form a bilayer. The bilayer is covered by another polyester film as an inextensible backing layer. Using cyclic and monotonic peeling tests, we characterize the interfacial fatigue and fracture behaviors of the bilayer. From the experimental data, we obtain the interfacial fatigue threshold (4.6J/m2) under cyclic peeling, the slow crack threshold (33.9J/m2) under monotonic peeling, and the adhesion toughness (~ 400J/m2) at a finite peeling speed. We develop a modified Lake-Thomas model to describe the interfacial fatigue threshold due to noncovalent bond breaking. The theoretical prediction (2.6J/m2) agrees well with the experimental measurement (4.6J/m2). Finally, we discuss possible additional dissipation mechanisms involved in the larger slow crack threshold and much larger adhesion toughness. It is hoped that this study will provide new fundamental knowledge for fracture mechanics of PSAs, as well as guidance for future tough and durable PSAs.

Free-standing polyaniline-reduced graphene oxide (PANI-rGO) thermoelectric films via electrochemical synthesis

Abstract Heat-based energy harvesting is gaining attention as an alternative energy source. Thermoelectric materials (TEs) generate voltages in response to a thermal gradient and conductive polymer-carbon composites have properties that make them favorable for these applications. Polyaniline-reduced graphene oxide (PANi-GO) thermoelectric thin films were fabricated by the electropolymerization of PANi with simultaneous co-deposition of graphene onto fluorine-doped tin oxide (FTO). Poly(butyl acrylate) was spin-coated onto these films as backing support to make a stable free-standing film of PANi-rGO. The free-standing film was formed upon GO reduction which resulted in simultaneous delamination from the FTO electrode. Compositional and morphological data were obtained via Raman microspectroscopy and scanning electron microscopy and the TE properties were measured in terms of the Seebeck coefficient and conductivities from Hall effect measurements. The Seebeck coefficients of the films measured between 6.6 μV K−1 to 13.4 μV K−1, whereas Hall effect conductivities ranged from 0.483 to 2.68 S cm−1. The highest film power factor measured was 0.025 μW m−1K−2. Varying the GO content used in the electropolymerized film did not have a significant effect on the overall TE property though varying the reduction cycle number and voltage resulted in significant changes in the film Seebeck coefficients and conductivities.

Natural Attenuation Potential of Vinyl Chloride and Butyl Acrylate Released in the East Palestine, Ohio Train Derailment Accident.

The East Palestine, Ohio train derailment released toxic vinyl chloride (VC) and butyl acrylate (BA), which entered the watershed. Streambed sediment, surface water, and private well water samples were collected 128 and 276 days postaccident to assess the natural attenuation potential of VC and BA by quantifying biodegradation biomarker genes and conducting microcosm treatability studies. qPCR detected the aerobic VC degradation biomarkers etnC in ∼40% and etnE in ∼27% of sediments collected in both sampling campaigns in abundances reaching 105 gene copies g-1. The 16S rRNA genes of organohalide-respiring Dehalococcoides and Dehalogenimonas were, respectively, detected in 50 and 64% of sediment samples collected 128 days postaccident and in 63 and 88% of sediment samples collected 276 days postaccident, in abundances reaching 107 cells g-1. Elevated detection frequencies of VC degradation biomarker genes were measured immediately downstream of the accident site (i.e., Sulphur Run). Aerobic VC degradation occurred in all sediment microcosms and coincided with increases of etnC/etnE genes and Mycobacterium, a genus comprising aerobic VC degraders. The conversion of VC to ethene and an increased abundance of VC reductive dechlorination biomarker genes were observed in microcosms established with sediments collected from Sulphur Run. All anoxic microcosms rapidly degraded BA to innocuous products with intermediate formation of n-butanol and acrylate. The results indicate that microbiomes in the East Palestine watershed have natural attenuation capacity for VC and BA. Recommendations are made to improve first-response actions in future contaminant release accidents of this magnitude.

Synthesis of Amphiphilic Polyacrylates as Peelable Coatings for Optical Surface Cleaning

Optical instruments require extremely high precision, and even minor surface contamination can severely impact their performance. Peelable coatings offer an effective and non-damaging method for removing contaminants from optical surfaces. In this study, an amphiphilic polyacrylate copolymer (PMLEA) was synthesized via solution radical copolymerization using the lipophilic monomer lauryl acrylate (LA) and hydrophilic monomers ER-10, methyl methacrylate (MMA), and butyl acrylate (BA). The structure and molecular weight of the copolymer were characterized using Fourier transform infrared spectroscopy (FTIR), nuclear magnetic resonance (NMR), and gel permeation chromatography (GPC). The hydrophilic–lipophilic balance, surface tension, and wettability of the copolymer were analyzed through water titration, the platinum plate method, and liquid contact angle tests. The cleaning performance of the copolymer coating on quartz glass surface contaminants was evaluated using optical microscopy and Ultraviolet-Visible Near-Infrared (UV-Vis-NIR) spectroscopy. The study examined the effect of varying the ratio of LA to ER-10 on the hydrophilicity, lipophilicity, cleaning efficiency, and mechanical properties of the copolymer coating. The results showed that when the mass ratio of LA to ER-10 was 1:2, the synthesized copolymer exhibited optimal performance in removing dust, grease, and fingerprints from quartz glass surfaces. The coating had a tensile strength of 2.57 MPa, an elongation at break of 183%, and a peeling force of 2.07 N m−1.

The Role of Starch Incorporation into Waterborne Acrylic-Hybrid Nanoparticles for Film-Forming Applications.

The use of biopolymers as an alternative to petroleum-based polymers offers a sustainable solution with benefits such as biodegradability and unique functionalities. In this study, starch/zein bioparticles (BPs) obtained by nanoprecipitation were employed to synthesize acrylic polymer/biopolymer waterborne nanoparticles with excellent film formation capability. These hybrid nanoparticle dispersions were obtained through a semibatch emulsion polymerization using the previously synthesized BPs as seed and variable monomeric formulations composed of butyl acrylate and methyl methacrylate. A synergetic effect between acrylic and biopolymer phases was evidenced where the incorporation of BPs had a fundamental role in improving sensitive properties, such as film blocking resistance, while attaining smooth films at room temperature. These excellent film-forming properties of starch/acrylic hybrid latexes without requiring the addition of formulation agents, which depict an important benefit from an environmental viewpoint, demonstrate that they represent a promising alternative for the development of a new generation of eco-friendly binders.

Study on UV-Curable Acrylic Clear Viscoelastic Materials with Grafted Structures

Flexible substrates are crucial for wearable electronic strain sensors, but achieving biocompatibility, low cost, and aesthetic appeal alongside good mechanical performance remains challenging. Acrylic-based clear viscoelastic films (CVFs) are gaining attention due to their excellent transparency and potential for enhanced mechanical properties. This study synthesized copolymers CVF1-4 with varying branch content using soft monomers 2-ethylhexyl acrylate (2-EHA), butyl acrylate (n-BA), and functional monomer acrylic acid (AA). Employing a "grafting-through" strategy, small molecule monomers, ATRP-synthesized oligomer pBA25, and photoinitiator 1,6-hexanediol diacrylate (HDDA) were in-situ polymerized under UV light to form transparent, flexible elastic films CVF1-4. Between -20 to 80 C, CVF1-4 demonstrated excellent mechanical properties such as low modulus (in the kPa range), low glass transition temperature (below -20 C), large deformation (500-600%), and high strain recovery rate (>95%). Among them, CVF3 with 15% branching showed a balanced comprehensive performance, exhibiting primarily elastic behavior at room temperature. Therefore, selecting appropriate molecular composition and grafting structure provides a simple and customizable solution for optimizing CVF properties.

Photo-induced time-dependent controllable wettability of dual-responsive multi-functional electrospun MXene/polymer fibers

Switchable wettability potential in smart fibers is of paramount importance in various applications. Light-induced controllable changes in surface wettability have a significant role in this area. Herein, smart waterborne homopolymer, functional copolymer with different polarity and flexibility, and multi-functional terpolymer particles containing a time-dependent dual-responsive acrylated spiropyran, as a polymerizable monomer, were successfully synthesized through eco-friendly single-step emulsifier-free emulsion polymerization. Presence of 10 wt% of butyl acrylate and dimethylaminoethyl methacrylate relative to methylmethacrylate as functional comonomers decreased the Tg of the samples almost 20 ℃ and increased their polarity. The optical properties of the particles were investigated, and the UV–vis and fluorescence spectroscopy results showed that not only polarity and flexibility of the polymer chains may have a positive effect on improving the optical properties, but also the simultaneous presence of functional groups has a synergistic effect. The smart polymer particles with flexibility and polarity features exhibited higher absorption and emission compared to other samples. Inspired by these findings, multi-functional smart polymer fibers were prepared using the electrospinning method. The smart multi-functional electrospun fibers containing few-layer Ti3C2 MXenes were synthesized to improve the fibers’ properties and change the surface wettability due to the hydrophilic functional groups of MXene. Field-emission scanning electron microscopy images displayed the successful preparation of few-layer MXenes. Smooth and bead-free fibers with bright red fluorescence emission under UV irradiation were shown using fluorescence microscopy. The study on the surface wettability of fibers revealed that UV and visible light irradiation induced reversible time-dependent changes in the wettability of the smart multi-functional MXene/polymer electrospun fibers from hydrophobic to hydrophilic, reaching a water contact angle of 10° from an initial water contact angle of 100° under UV light and also changing to superhydrophilic state with passing time. Upon visible light exposure, the fibers returned to their original state. Furthermore, the fibers demonstrated a high stability over five alternating cycles of UV and visible light irradiation. This study shows that the fabrication of time-dependent smart fibers, utilizing the flexibility and polarity in the presence of MXenes, significantly improves and controls surface wettability changes. The outstanding dynamically photo-switchable wettability of these fibers may offer exciting opportunities in various applications, especially in the separation of oil from water contaminants.

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.

Low-tortuosity, high-loading electrodes for fast-charging quasi-solid-state lithium metal batteries

Structural design of electrodes is a widely adopted approach towards enhanced electrochemical performance in various battery systems. However, in quasi-solid-state lithium metal batteries, research has predominantly focused on developing gel polymer electrolytes (GPEs), with limited attention given to utilizing electrodes with specialized structural design. Herein, by exploiting the excellent wettability and permeability of the GPE, high-loading NMC-811 cathodes featuring aligned channels achieved through freeze-casting are integrated with in-situ UV-polymerized poly (butyl acrylate) (PBA). The aligned channels in the freeze-cast electrodes provide low-tortuosity pathways for smooth Li+ transport, facilitating rapid kinetics. Consequently, superior areal capacity can be delivered under high areal current density (e.g. 1 mAh cm−2 at 2 mA cm−2 and 0.7 mAh cm−2 at 3.8 mA cm−2), demonstrating the fast-charging capability of quasi-solid-state lithium metal batteries.

Reusable pyrene-based fluorescent organogels for polychlorinated biphenyl detection and removal

Highly toxic hydrophobic polychlorinated biphenyls (PCBs) pollutants are resistant to degradation, and limited methods are available for their elimination, leading to their long-term persistence in ecosystems, which can harm humans and the environment. Therefore, early detection, removal, and continuous monitoring of PCBs are crucial. In this study, a novel fluorescent polymeric probe (P1) to detect PCB congeners (77, 118, and 126) in water was developed. P1 was synthesized by incorporating N,N’-dimethylacrylamide (DMAA) and pyren-1-ylmethyl methacrylate (PyMMA) to form p(DMAA-co-PyMMA). P1 demonstrated high sensitivity toward the most toxic coplanar PCB congeners, 77 and 126, via a fluorescence turn-on mechanism. This sensitivity was attributed to hydrophobic and π–π interactions between the PCBs and PyMMA units of P1. The detection limits for PCB congeners 77 and 126 were determined to be 0.028 and 0.039 mM, respectively. However, PCB 118, a mixed planar congener, exhibited less detection sensitivity than PCB 77 and 126. A porous three-dimensional polymeric organogel (OG) comprising butyl acrylate, PyMMA, and a cross-linker ethylene glycol dimethacrylate was synthesized for practical application. The OG selectively removed PCBs compared to other competing pollutants due to the high hydrophobicity of the PCBs, achieving removal rates of 63 % for PCB 77 and 55 % for PCB 126. The large surface area of the OG facilitated enhanced hydrophobic and π-π interactions between the PCBs and pyrene units. This work emphasizes the efficacy of P1 in detecting PCBs and the potential of using OG in eliminating PCBs, offering a viable method for monitoring and remedying PCB-contaminated environments.

Ultrasonic Velocity of Acrylates with Decane-2-ol at 313.15 K

Thermodynamic data involving ultrasonic velocities of binary liquid mixtures of methyl acrylate, ethyl acrylate and butyl acrylate with decane-2-ol have been measured at 313.15 K and at atmospheric pressure. Study of thermodynamic properties involves challenges of interpreting the excess quantities as a means of understanding the nature of intermolecular interactions among the mixed components. Experimental values of ultrasonic velocities were correlated with recently proposed Jouyban-Acree model. Deviations in isentropic compressibility were calculated and have been fitted to Redlich-Kister polynomial equation. Excess parameters like specific acoustic impendence, intermolecular free length, available volume, intrinsic pressure, molecular association and molar sound velocity were also calculated. Graphical representations of excess derived thermodynamic parameters used to explain the type and extent of intermolecular interactions

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.

Microstructural analysis and characterization of poly(butyl acrylate) grafted silicone rubber synthesized via reverse ATRP

Microstructural analysis and characterization of poly(butyl acrylate) grafted silicone rubber synthesized via reverse ATRP

Neutron and X-ray Scattering Characterization of Silica Nanoparticle-Stabilized Polymer Hybrid Latex Particles.

A robust route to produce poly(methyl methacrylate) (pMMA) hybrid latex particles (radius ∼250 nm) that are selectively "armored" with silica nanoparticles (radius 12.5 nm) through addition of vinyltriethoxysilane was previously shown ( J. Colloid Interface Sci. 2018, 528, 289-300).Depending on synthesis conditions, the extent of nanoparticle attachment could be varied; however, the mechanism behind this attachment during latex growth remained unclear. The dual population of particles present (silica + polymer) means that particle sizing by dynamic light scattering is ambiguous. Furthermore, the low glass transition temperature (Tg) of polymers such as poly(butyl acrylate) (pBA) typically used in film-forming applications for decorative coatings (i.e., paints) means that the hybrid latex particles are too "soft" for robust analysis through atomic force microscopy (AFM) and scanning electron microscopy (SEM). Here, we show that small- and ultrasmall-angle neutron scattering (SANS and USANS), along with complementary data from small-angle X-ray scattering (SAXS), reveals that these armored hybrid latex particles adopt a raspberry-type configuration, supporting their core-shell structure. The number of nanoparticles present on the surface of the hybrid latex can be adjusted by addition of one of a diverse range of alkyl- or perfluoroalkyl-silanes to alter silica nanoparticle hydrophobicity, and quantified through analysis of scattering data. The approach therefore provides a novel, nonperturbative, and in situ method of quantifying nanoparticle attachment to polymer latex particles.