Search Results (18)

A novel mesoporous spherical chelating lignin-based adsorbent was successfully synthesized via inverse suspension polymerization using sulfate pine pulping black liquor as raw material, followed by graft copolymerization with acrylonitrile and subsequent amination. The obtained aminated cyanoethyl spherical lignin resin (ACSLR) exhibited a well-defined porous morphology and abundant active sites, as confirmed by SEM and FT-IR. Adsorption experiments demonstrated high Pb²⁺ uptake capacity (63.98 mg·g⁻¹) under optimal conditions (pH = 5.5, 2.0 g·L⁻¹ adsorbent dosage, and 150 mg·L⁻¹ initial concentration of Pb²⁺ solution). The adsorption process followed the Langmuir isotherm and pseudo-second-order kinetics, indicating monolayer chemisorption dominated by amino and cyano groups. This work provides a sustainable strategy for valorizing industrial lignin waste into efficient adsorbents for heavy metal removal, highlighting its potential for practical wastewater treatment applications. Full article

Due to the high formation temperature of high-temperature reservoirs, ordinary polyacrylamide microspheres cannot meet the requirements for temperature resistance. To address the challenge of deep profile control in high-temperature reservoirs, we prepared AM/PF polymer microspheres with excellent temperature resistance through the copolymerization of water-soluble phenolic resin (PF) and acrylamide (AM). The swelling properties of AM/PF polymer microspheres were examined using a visible light microscope, SEM, and laser diffraction. The plugging and migration characteristics of the microspheres were evaluated using membrane filtration tests and sand-filled tube displacement tests. The results indicate that the average particle size of AM/PF microspheres prepared via inverse suspension polymerization is approximately 30 μm, and the swelling process is relatively slow. The microspheres take approximately 15 days to fully swell, with a volume swelling ratio of roughly 34.25. At high temperatures, the swollen microsphere dispersion system can effectively block microporous membranes with specific pore sizes. As the concentration of microspheres increases, their plugging effect gradually enhances; however, this effect diminishes as permeability increases. The AM/PF polymer microspheres exhibit excellent temperature stability along with favorable plugging and migration characteristics at specific permeabilities. Full article

This study introduces fluorescent polymer gel microspheres (FPMs) as a novel approach to enhance conformance control in oil reservoirs. Designed to address the challenges of high-permeability zones, FPMs were synthesized via inverse suspension polymerization, incorporating 2-acrylamido-2-methylpropane sulfonic acid (AMPS) to improve thermal stability and swelling and fluorescein to enable fluorescence. Characterization using FT-IR, SEM, fluorescence spectroscopy, and thermal analysis revealed that FPMs swell significantly in brine, with diameters increasing from 46 μm to 210 μm, and maintain thermal stability up to 110 °C. These advanced properties make FPMs highly effective in reducing permeability and facilitating real-time tracking, offering a promising solution for improved oil recovery and efficient reservoir management. Full article

Control of the porous structure and particle size is essential for improving the properties of polysilsesquioxane (PSQ) microspheres. Herein, using the strategy combining inverse suspension polymerization, two-step sol–gel- and polymerization-induced phase separation processes, micron-sized thiol-containing macroporous PSQ (TMPSQ) microspheres with controllable morphologies, adjustable particle diameters (4.9–17.3 μm), and pore sizes (40–3774 nm) were prepared. The morphology and size of the TMPSQ microspheres were characterized by SEM. The mercury intrusion method was employed to analyze the porous structure of the microspheres. The effects of the composition of the sol–gel disperse phase, the mass ratio of the sol–gel disperse phase to the oil continuous phase (WR_W/O), and the Span 80 mass content in the oil continuous phase on the morphology, particle diameter and pore size of the TMPSQ microspheres were investigated. Results indicated that the composition of the sol–gel disperse phase determines the morphology and porous structure of the microspheres, and WR_W/O and Span 80 content have remarkable impacts on the morphology and particle size of the microspheres. This study is beneficial to the design and fabrication of functional PSQ microspheres with desired properties and promising application prospects. Full article

This paper focuses on the preparation and evaluation of a novel humidity-control material, vermiculite/(sodium polyacrylate(AA)–acrylamide(AM)), using inverse suspension polymerization. Acrylic acid and acrylamide were introduced into the interlayer of modified vermiculite during the polymerization process, leading to the formation of a strong association with the modified vermiculite. The addition of vermiculite increased the specific surface area and pore volume of the composites. To investigate the moisture absorption and desorption properties of the composites, an orthogonal experiment and single-factor experiment were conducted to analyze the impacts of vermiculite content, neutralization degree, and the mass ratio of AA to AM. According to the control experiment, the addition of vermiculite was found to enhance the pore structure and surface morphology of the composite material, surpassing both vermiculite and PAA-AM copolymer in terms of humidity control capacity and rate. The optimal preparation conditions were identified as follows: vermiculite mass fraction of 4 wt%, a neutralization degree of 90%, and m_AA:m_AM = 4:1. The moisture absorption rate and moisture release rate of the composite material prepared under these conditions are 1.285 g/g and 1.172 g/g. The humidity control process of the composite material is governed by pseudo second-order kinetics, which encompasses the complete adsorption process. These results indicate that the vermiculite/PAA-AM composite humidity control material has excellent humidity control performance and is a simple and efficient humidity control method. Full article

Polysilsesquioxane (PSQ) microspheres have shown promise in many fields, but previous studies about porous PSQ microspheres are scarce. Herein, we fabricated novel micron-sized thiol-functional polysilsesquioxane (TMPSQ) microspheres with open and interconnected macropores by combining inverse suspension polymerization with two-step sol–gel and polymerization-induced phase separation processes, without using phase-separation-promoting additives or sacrificial templates. The chemical composition of the TMPSQ microspheres was confirmed using FTIR and Raman spectroscopy. The morphology of the TMPSQ microspheres was characterized using SEM and TEM. TGA was employed to test the thermal stability of the TMPSQ microspheres. Mercury intrusion porosimetry and nitrogen adsorption–desorption tests were performed to investigate the pore structure of the TMPSQ microspheres. The results showed that the TMPSQ microspheres had open and interconnected macropores with a pore size of 839 nm, and the total porosity and intraparticle porosity reached 70.54% and 43.21%, respectively. The mechanism of porous generation was proposed based on the morphological evolution observed using optical microscopy. The macropores were formed through the following four steps: phase separation (spinodal decomposition), coarsening, gelation, and evaporation of the solvent. The macropores can facilitate the rapid mass transfer between the outer and inner spaces of the TMPSQ microspheres. The TMPSQ microspheres are promising in various fields, such as catalyst supports and adsorbents. Full article

Although biodegradable microgels represent a useful drug delivery system, questions remain regarding the kinetics of gel degradation and subsequent drug release. Spherical microgels (~Ø10–300 µm) were synthesized using an inverse suspension polymerization method. Specifically, acrylamide and acrylonitrile monomers were thermally co-polymerized with N,N’-bis(acryloyl)cystamine as a cross-linker with disulfide bridges. The kinetics and mechanism of degradation of these cross-linked, degradable, fluorescently labeled microgels (PAAm-AN-BAC-FA) were quantitatively studied under confocal microscopy at various concentrations of glutathione (reducing agent) ranging from 0.06 to 91.8 mM. It was found that polymer network degradation via the cleavage of disulfide bonds was accompanied by two overlapping processes: diffusion-driven swelling and dissolution-driven erosion. A slow increase in microgel size (swelling) resulted from partial de-cross-linking in the bulk of the microgel, whereas a faster decrease in fluorescence intensity (erosion) resulted from the complete cleavage of disulfide bonds and the release of uncleaved polymeric chains from the microgel immediate surface into the solution. Swelling and erosion exhibited distinct kinetics and characteristic times. Importantly, the dependence of kinetics on glutathione concentration for both swelling and erosion suggests that degradation would occur faster in cancer cells (higher concentration of reductants) than in normal cells (lower concentration of reductants), such that drug release profiles would be correspondingly different. A greater comprehension of microgel degradation kinetics would help in (i) predicting the drug release profiles for novel multifunctional drug delivery systems and (ii) using redox-sensitive degradable hydrogel particles to determine the concentrations of reducing agents either in vitro or in vivo. Full article

Porous materials can be found in numerous essential applications. They are of particular interest when, in addition to their porosity, they have other advantageous properties such as thermal stability or chemical diversity. The main aim of this study was to synthesize the porous copolymers of 9,10-bis(methacryloyloxymethyl)anthracene (BMA) with three different co-monomers divinylbenzene (DVB), ethylene glycol dimethacrylate (EGDMA) and trimethylpropane trimethacrylate (TRIM). They were synthesized via suspension polymerization using chlorobenzene and toluene served as porogenic solvents. For the characterization of the synthesized copolymers ATR-FTIR spectroscopy, a low-temperature nitrogen adsorption–desorption method, thermogravimetry, scanning electron microscopy, inverse gas chromatography and size distribution analysis were successfully employed. It was found that depending on the used co-monomer and the type of porogen regular polymeric microspheres with a specific surface area in the range of 134–472 m²/g can be effectively synthesized. The presence of miscellaneous functional groups promotes divergent types of interactions Moreover, all of the copolymers show a good thermal stability up to 307 °C. What is important, thanks to application of anthracene derivatives as the functional monomer, the synthesized materials show fluorescence under UV radiation. The obtained microspheres can be used in various adsorption techniques as well as precursor for thermally resistant fluorescent sensors. Full article

Photonic crystals (PCs) are nanomaterials with photonic properties made up of periodically modulated dielectric materials that reflect light between a wavelength range located in the photonic band gap. Colloidal PCs (C-PC) have been proposed for several applications such as optical platforms for the formation of physical, chemical, and biological sensors based on a chromatic response to an external stimulus. In this work, a robust protocol for the elaboration of photonic crystals based on SiO₂ particle (SP) deposition using the vertical lifting method was studied. A wide range of lifting speeds and particle suspension concentrations were investigated by evaluating the C-PC reflectance spectrum. Thinner and higher reflectance peaks were obtained with a decrease in the lifting speed and an increase in the SP concentrations up to certain values. Seven batches of twelve C-PCs employing a SP 3% suspension and a lifting speed of 0.28 µm/s were prepared to test the reproducibility of this method. Every C-PC fabricated in this assay has a wavelength peak in a range of 10 nm and a peak width lower than 90 nm. Inverse-opal polymeric films with a highly porous and interconnected morphology were obtained using the developed C-PC as a template. Overall, these results showed that reproducible colloidal crystals could be elaborated on a large scale with a simple apparatus in a short period, providing a step forward in the scale-up of the fabrication of photonic colloidal crystal and IO structures as those employed for the elaboration of photonic polymeric sensors. Full article

Objectives: The intranasal route represents a high promising route of administration aiming for brain delivery. Yet, it represents one of the most difficult and complicated routes. Accordingly, scientists are in a continuous search for novel drug delivery vehicles such as the lipid and polymeric nanoparticles that are apt to enhance the bioavailability of the administered drugs to reach the brain. In this study, a certain number of publications were selected from different databases and literature. Meta-analysis studies using two different algorithms (DerSimonian–Laird and inverse variance) followed aiming to explore the published studies and confirm by evidence the superiority of nanocarriers in enhancing the brain bioavailability of various drugs. Furthermore, the quantitative comparison of lipid versus polymeric nanosystems was performed. Methods: The area under the curve (AUC) as an important pharmacokinetic parameter extracted from in vivo animal studies was designated as the “effect” in the performed meta-analysis after normalization. Forest plots were generated. Key findings and Conclusions: The meta-analysis confirmed the augmentation of the AUC after the comparison with traditional preparations such as solutions and suspensions. Most importantly, lipid nanoparticles were proven to be significantly superior to the polymeric counterparts. Full article

Poly(amidoamine)s (PAMAM) are very effective in the removal of heavy metal ions from water due to their abundant amine and amide functional groups, which have a high binding ability to heavy metal ions. We synthesized a new class of hyperbranched poly(amidehydrazide) (PAMH) hydrogel particles from dihydrazides and N,N′-methylenebisacrylamide (MBA) monomer by using the A2 + B4 polycondensation reaction in an inverse suspension polymerization process. In Cd²⁺ and Cu²⁺ ion sorption tests, the synthesized dihydrazide-based PAMH hydrogel particles exhibited sorption capacities of 85 mg/g for copper and 47 mg/g for cadmium. Interestingly, the PAMH showed only a 10% decrease in sorption ability in an acidic condition (pH = 4) compared to the diamine-based hyperbranched PAMAM, which showed a ~90% decrease in sorption ability at pH of 4. In addition, PAMH hydrogel particles remove trace amounts of copper (0.67 ppm) and cadmium (0.5 ppm) in water, below the detection limit. Full article

Oleic acid (OA)-modified Fe₃O₄ nanoparticles were successfully covered with polyanilines (PANIs) via inverse suspension polymerization in accordance with SEM and TEM micrographs. The obtained nanoparticles were able to develop into a ferrite (α-Fe) and α″-Fe₁₆N₂ mixture with a superparamagnetic property and high saturated magnetization (SM) of 245 emu g⁻¹ at 950 °C calcination under the protection of carbonization materials (calcined PANI) and other iron-compounds (α″-Fe₁₆N₂). The SM of the calcined iron-composites slightly decreases to 232 emu g⁻¹ after staying in the open air for 3 months. The calcined mixture composite can be ground into homogeneous powders without the segregation of the iron and carbon phases in the mortar without significantly losing magnetic activities. Full article

In this study, the synthesis and characterization of permanently porous polymeric microspheres was presented. The microspheres were obtained via suspension polymerization using diverse functional monomers, such as 4,4′-bis(methacryloyloxymethylphenyl)sulphone, 1,4-bis(methacryloyloxymethyl)benzene, 4,4′-bis(methacryloyloxymethylphenyl)methane, N-vinylpyrrolidone, ethylene glycol dimethacrylate, and divinylbenzene as a co-monomer. As porogenic solvents, toluene and chlorobenzene were applied. The main aim of the research was to synthesize polymers having a highly developed internal structure and a good thermal stability. The synthesized materials were characterized by ATR-FTIR, scanning electron microscopy, a size distribution analysis, a low-temperature nitrogen adsorption–desorption method, differential scanning calorimetry, and thermogravimetry coupled with FTIR and inverse gas chromatography. It was found that, depending on the functional monomer, regular microspheres with a specific surface area in the range of 418–746 m²/g can be successfully synthesized. Moreover, all the synthesized copolymers showed a good thermal stability. In helium, they exhibited 5% mass losses at temperatures over 300 °C, whereas in air these values were only slightly lower. In addition, the presence of miscellaneous functional groups promoted diverse kinds of interactions. Therefore, the microspheres can be possibly use in many adsorption techniques including high temperature processes. Full article

Superabsorbent polymer (SAP) particles are primarily applied for absorbing and storing liquids. Here, poly (acrylic acid) (PAA)-based SAP microspheres incorporated with silver nanoparticles (AgNPs) are prepared as an effort to maintain microsphere shape during swelling and minimize gel blocking. PAA-based SAP spheres are synthesized via inverse suspension polymerization. AgNPs are formed within SAP spheres through in situ reduction of silver nitrate (AgNO₃), using polyvinylpyrrolidone as the reducing agent. The formation of AgNPs within SAP was observed via techniques such as scanning electron microscopy, ultraviolet-visible spectroscopy, thermogravimetric analysis, X-ray photoelectron spectroscopy and transmission electron microscopy. Energy dispersive spectroscopy analyses reveal that thin and dense layers of AgNPs are formed on the outer regions of the SAP spheres at higher concentrations of AgNO₃. The water absorbency capacity decreases on increasing the amount of incorporated silver nanoparticles; however, it is comparable with that of commercially available surface-crosslinked SAP particles. Finally, micro-computerized tomography (micro-CT) study revealed that AgNP-incorporated SAP spheres maintained their shapes during swelling and exhibit higher void fractions in the packed gel bed, minimizing gel blocking and improving fluid permeability. Full article

Micrometer-sized hyperbranched poly(amidoamine) (hPAMAM) particles are prepared with a simple A₂B₃ type Aza–Michael addition reaction between aminoethylpiperazine (AEP) and methylenebisacrylamide (MBA) in an inverse suspension polymerization condition. The synthesized particles exhibited surprisingly high Cu²⁺ sorption capacity (0.223g/g) for a solid-type absorbent. In addition to the high sorption ability of the particle, its simple synthetic process and convenience, due to its micrometer-sized spherical shape and recyclability, make it a practical and attractive absorbent for heavy metal ion removal from aqueous solutions. Full article