Search Results (188)

Sulfur-containing polymers are unique sustainable materials with promise for the development of various adsorbents for environmental remediation. However, they have not been explored for CO₂ capture despite reports on its ability to decontaminate various aqueous pollutants. This study reports on the single-step synthesis of a diamine-functionalized sulfur-containing copolymer by the thermally induced radical copolymerization of N2,N2-Diallylmelamine (NDAM), a difunctional monomer, with sulfur and explores its use for CO₂ capture. The influence of reaction parameters such as the weight ratios of sulfur to NDAM, reaction temperature, time, and the addition of a porogen on the properties of aminated copolymer was investigated. The resulting copolymers were characterized using FTIR, TGA, DSC, SEM, XRD, and BET surface area analyses. The incorporation of NDAM directly imparted amine functionality while stabilizing the polysulfide chains by crosslinking, leading to a thermoset copolymer with an amorphous structure. The addition of a NaCl particle porogen to the S/NDAM mixture generated a mesoporous structure, enabling the resulting copolymer to be tested for CO₂ adsorption under varying pressures, leading to an adsorption capacity as high as 517 mg/g at 25 bar. This work not only promotes sustainable hybrid materials that advance green chemistry while aiding CO₂ mitigation efforts but also adds value to the abundant amount of sulfur by-products from petroleum refineries. Full article

The development of ultraflexible and sensitive gas sensors is critical for advancing next-generation environmental monitoring and healthcare diagnostics. In this work, we demonstrate an ultraflexible chemiresistive nitrogen dioxide (NO₂) sensor integrated with a photopatterned porous poly(3-hexylthiophene) (P3HT)/SU-8 blend film as an active sensing layer. The porous microarchitecture was fabricated via high-resolution photolithography, utilizing SU-8 as a photoactive porogen to template a uniform, interconnected pore network within the P3HT matrix. The engineered porosity level ranged from 0% to 36%, substantially improving gas diffusion kinetics to enlarge the accessible surface area for analyte adsorption. Our sensor exhibited a marked enhancement in sensitivity at an optimized porosity of 36%, with the current response at 30 ppm NO₂ increasing from 354% to 3201%, along with a detection limit of 0.7 ppb. The device further exhibited a high selectivity against common interfering gases, including NH₃, H₂S, and SO₂. Moreover, the porous structure imparted excellent mechanical durability, maintaining over 90% of its initial sensing performance after 500 bending cycles at a 1 mm radius, underscoring its potential for integration into next-generation wearable environmental monitoring platforms. Full article

Porous PZT films offer significant potential due to tunable electromechanical properties, yet the polarization behavior remains insufficiently understood because of discontinuous morphology and domain structures. In this work, we study the impact of porosity on the spontaneous polarization and electromechanical response of PZT thin films fabricated using a multilayer spin-coating technique with various concentrations (0–14%) of polyvinylpyrrolidone (PVP) as a porogen. Atomic force microscopy (AFM) and piezoresponse force microscopy (PFM) were employed to analyze the local topography, domain distribution, and polarization behavior of the films. The results indicate that increasing porosity leads to substantial changes in grain morphology, dielectric permittivity, and polarization response. Films with higher porosity exhibit a more fragmented polarization distribution and reduced piezoresponse, while certain orientations demonstrate enhanced domain mobility. Despite the decrease in overall polarization, the local coercive field remains relatively stable, suggesting structural stability during the local polarization switching. The findings highlight the crucial role of grain boundaries and local charge redistribution in determining local polarization behavior. Full article

Developing scaffolds with a three-dimensional porous structure and adequate mechanical properties remains a key challenge in tissue engineering of bone. These scaffolds must be biocompatible and biodegradable to effectively support osteoblastic cell attachment, metabolic activity, and differentiation. This study successfully fabricated a chitosan–bacterial cellulose (CS–BC) composite scaffold using the solvent casting/particle leaching (SCPL) technique, with NaOH/urea solution and sodium chloride crystals as the porogen. The scaffold exhibited a well-distributed porous network with pore sizes ranging from 300 to 500 µm. Biodegradation tests in PBS containing lysozyme revealed a continuous degradation process, while in vitro studies with MC3T3-E1 cells (pre-osteoblastic mouse cell line) demonstrated excellent cell attachment, as observed through SEM imaging. The scaffold also promoted increased metabolic activity (OD values) in the MTT assay, and enhanced alkaline phosphatase (ALP) activity and upregulated expression of osteogenic-related genes. These findings suggest that the CS–BC composite scaffold, fabricated using the SCPL method, holds great potential as a candidate for bone tissue engineering applications. Full article

The versatility of molecularly imprinted polymers (MIPs) has led to their integration into applications like biosensing, separation, environmental monitoring, and drug delivery technologies. This diversity of applications has resulted in a plethora of synthesis approaches to precisely tailor the materials’ properties to the specific demands. A critical, yet often overlooked, factor in MIP synthesis is the choice of porogen. Porogens play a pivotal role in defining the morphology, surface properties, swelling behavior, and binding efficiencies of the resulting MIPs. While aprotic solvents have traditionally been the standard in molecular imprinting, recent developments have expanded the variety of employed porogens accompanied by notable improvements in MIP performance. Therefore, this review aims to highlight both traditional and emerging types of porogens used in molecular imprinting, their influence on polymer properties and sorption performance, and their application across various sensing and extraction applications. Full article

Modern tissue engineering requires not only degradable materials promoting cell growth and differentiation, but also vascularization of the engineered tissue. Porous polylactide/polycaprolactone (PLA/PCL, ratio 3/5) foam scaffolds were prepared by a combined porogen leaching and freeze-drying technique using NaCl (crystal size 250–500 µm) and a water-soluble cellulose derivative (Klucel^TM E; 10–100% w/w relative to the total PLA/PCL concentration) as porogens. Scanning electron microscopy, micro-CT, and Brunauer–Emmett–Teller analysis showed that all scaffolds contained a trimodal range of pore sizes, i.e., macropores (average diameter 298–539 μm), micropores (100 nm to 10 μm), and nanopores (mostly around 3.0 nm). All scaffolds had an open porosity of about 90%, and the pores were interconnected. The size of the macropores and the nanoporosity were higher in the scaffolds prepared with Klucel. Nanoporosity increased water uptake by the scaffolds, while macroporosity promoted cell ingrowth, which was most evident in scaffolds prepared with 25% Klucel. Human adipose-derived stem cells co-cultured with endothelial cells formed pre-vascular structures in the scaffolds, which was further enhanced in a dynamic cell culture system. The scaffolds are promising for the engineering of pre-vascularized soft tissues (relatively pliable 10% Klucel scaffolds) and hard tissues (mechanically stronger 25% and 50% Klucel scaffolds). Full article

Hierarchical zeolites with micro- and mesoporous frameworks can overcome diffusional limitations of microporous systems. This study investigates the post-synthetic modification of Beta zeolite using different porogeneous agents (NaOH, NH₄OH, NH₄F) under identical conditions to compare their efficiency in generating mesopores. The effect of treatment time was also examined for NH₄OH and NH₄F. The modified materials were characterized using physicochemical techniques and evaluated for catalytic performance in acetic acid esterification with alcohols of different sizes and adsorption of methylene blue. All the modifications increased mesoporosity but reduced acidity. NaOH produced the highest mesoporosity but significantly reduced acidity, while NH₄F retained the most acidity. Catalytic activity in esterification with methanol depended on acidity, but for larger alcohols (n-butanol, benzyl alcohol), activity was influenced by both acidity and mesoporosity. The NH₄OH- and NH₄F-modified materials, with lower mesoporosity but higher acidity, exhibited better performance with larger alcohols. In MB adsorption, the adsorption equilibrium rates increased with mesoporosity. The NaOH-modified sample reached equilibrium the fastest due to its superior mesoporosity, while the NH₄F-modified sample demonstrated the highest adsorption efficiency owing to its abundant Brønsted acid sites. These findings demonstrate that the choice of modifier affects mesoporosity, acidity, and functional performance, offering insights into tailoring hierarchical zeolites for specific applications. Full article

Cranio-maxillofacial bone reconstruction, especially for large defects, remains challenging. Synthetic biomimetic materials are emerging as alternatives to autogenous grafts. Tissue engineering aims to create natural tissue-mimicking materials, with calcium phosphate-based scaffolds showing promise for bone regeneration applications. This study developed a porous calcium metaphosphate (CMP) scaffold with physicochemical properties mimicking natural bone, aiming to create a prevascularized synthetic bone graft. The scaffold, fabricated using sintered monocalcium phosphate with poly (vinyl alcohol) as a porogen, exhibited pore sizes ranging from 0 to 400 μm, with the highest frequency between 80 and 100 μm. The co-culture of endothelial cells (ECs) with human alveolar osteoblasts (aHOBs) on the scaffold led to the formation of tube-like structures and intrinsic VEGF release, reaching 10,455.6 pg/mL This level approached the optimal dose for vascular formation. Conversely, the co-culture with mesenchymal stem cells did not yield similar results. Combining ECs and aHOBs in the CMP scaffold offers a promising approach to developing prevascularized grafts for cranio-maxillofacial reconstruction. This innovative strategy can potentially enhance vascularization in large tissue-engineered constructs, addressing a critical limitation in current bone regeneration techniques. The prevascularized synthetic bone graft developed in this study could significantly improve the success rate of maxillofacial reconstructions, offering a viable alternative to autogenous grafts. Full article

Rosmarinic acid (RA) is a natural active compound widely found in many plants belonging to the family of Lamiaceae, Boraginaceae, and so on, which has various important bioactivities, including being anti-oxidative, anti-inflammatory, antiviral, etc. Herein, novel hydrophilic magnetic molecularly imprinted polymers (HMMIPs) with a regular core-shell structure were successfully developed using RA as a template molecule, acrylamide (AM) as a functional monomer, N-N ’methylenebisacrylamide (MBA) as a cross-linking agent, and water as the porogen. After a series of characterization and adsorption performance analyses, it was found that HMMIPs are hydrophilic with an adsorption capacity of 8.012 ± 0.54 mg/g, an imprinting factor of 3.64, and a selectivity coefficient of 2.63~2.91. Furthermore, the HMMIPs can be rapidly separated from other components under the influence of external magnetic fields. The HMMIPs were employed for the determination of RA present in the Perilla frutescens and Rosmarinus officinalis aqueous extract with recoveries of 88.2~107.3%. These results indicated that HMMIPs of RA have the benefits of straightforward operation, rapid adsorption, and high selectivity, rendering it an appropriate way for the expedient and selective isolation of RA in an intricate matrix. Full article

In this study, new monolithic poly(9-anthracenylmethyl methacrylate-co-trimethylolpropane trimethacrylate (TRIM) columns, referred as ANM monoliths were prepared, for the first time, and were used for the separation media for biomolecules and proteomics analysis by nano-liquid chromatography (nano-LC). Monolithic columns were prepared by in situ polymerization of 9-anthracenylmethyl methacrylate (ANM) and trimethylolpropane trimethacrylate (TRIM) in a fused silica capillary column of 100 µm ID. Polymerization solution was optimized in relation to monomer and porogenic solvent. Scanning electron microscopy (SEM) and chromatographic analyses were performed for the characterization studies of ANM monoliths. The ANM monolith produced more than 46.220 plates/m, and the chromatographic evaluation of the optimized ANM monolith was carried out using homologous alkylbenzenes (ABs) and polyaromatic hydrocarbons (PAHs), allowing both strong hydrophobic and π-π interactions. Run-to-run and column-to-column reproducibility values were found as <2.91% and 2.9–3.2%, respectively. The final monolith was used for biomolecule separation, including both three dipeptides, including Alanine-Tyrosine (Ala-Tyr), Glycine-Phenylalanine (Gly-Phe), and L-carnosine and five standard proteins, including ribonuclease A (RNase A), α-chymotrypsinogen (α-chym), lysozyme (Lys), cytochrome C (Cyt C), and myoglobin (Mb) in order to evaluate its potential. Both peptides and proteins were baseline separated using the developed ANM monolith in nano-LC. The ANM monolith was then applied to the protein and peptide profiling of MCF-7 cell line, which allowed a high-resolution analysis of peptides, providing a high peak capacity. Full article

Carboxymethyl cellulose sodium salt (CMC)-based superabsorbents are promising materials for the development of agricultural matrices aimed at water management and slow-release fertilizer production. However, an increase in the CMC content tends to reduce their water-absorbing capacity. This study aims to develop a cost-effective method for producing eco-friendly superabsorbents with enhanced water-absorbing capacity by incorporating a porogen and employing lyophilization. Superabsorbents containing 10 wt% CMC (CMC-SAPs) were synthesized via free radical polymerization with the addition of 0, 5, or 10 wt% ammonium carbonate as a porogen, followed by lyophilization. The synthesized CMC-SAPs were characterized using Fourier-transform infrared spectroscopy, scanning electron microscopy, thermogravimetric analysis, differential scanning calorimetry, and X-ray diffraction. The results revealed that CMC-SAPs prepared with the incorporation of a porogen and/or subjected to lyophilization exhibited well-developed surfaces featuring macropores and cavities. Incorporating 5 wt% ammonium carbonate as a porogen, followed by lyophilization, increased the equilibrium swelling ratio to 61%. This improvement was attributed to the enhanced surface morphology of the modified CMC-SAPs, which facilitated water molecule diffusion into the SAP matrix, as confirmed by open porosity measurements. This hypothesis was further supported by the diffusion coefficient values, which were higher for porogen-containing and lyophilized SAPs compared to unmodified samples. Moreover, the CMC-SAPs demonstrated good reusability. Thus, the combination of porogen incorporation and subsequent lyophilization represents a promising approach for enhancing the water uptake capacity of CMC-based composite superabsorbents for sustainable agricultural applications. Full article

Environmentally friendly nanoporous gels are tailor-designed and employed in the adsorption of toxic organic pollutants in wastewater. To ensure the maximum adsorption of the contaminant molecules by the gels, molecular modeling techniques were used to evaluate the binding affinity between the toxic organic contaminants such as methylene blue (MB) and Congo red (CR) and various biopolymers. To generate nanopores in the matrix of the polymeric gels, salt crystals were used as porogen. The pores were then used to accommodate catalytic nickel (Ni⁰) nanoparticles. Under UV irradiation, the nanoparticles demonstrated the effective adsorption and photocatalytic degradation of both the methylene blue and Congo red dyes, achieving removal efficiencies of up to 90% for MB and 80% for CR. The thermodynamic analysis suggested a spontaneous endothermic dissociative adsorption mechanism, which implies the oxidative catalytic degradation of the dyes. The kinetic modeling suggested a pseudo-second-order model, while the model for intra-particle diffusion revealed that Congo red diffuses faster than methylene blue. MB adsorption followed a Langmuir isotherm, while CR adsorption followed a linear isotherm. The results confirm that dye molecules initially undergo physisorption and subsequent dissociative adsorption. The products of the catalytic degradation of methylene blue continue to be absorbed on the surface of the nanoparticles, while those of Congo red switch to preferential desorption. Full article

Polyvinyl alcohol (PVA), possessing a strong ability to form hydrogels, has been widely used for various pharmaceutical and biomedical applications. In particular, the use of PVA-PEG in the form of theta gels for altered cartilage treatment has attracted an enormous amount of attention in the last 20 years. In this paper, we prepared 42 PVA-PEG in the form of theta gels at room temperature in an aqueous environment, testing the crystallization occurrence at basic pH (10 or 12). Using a statistical approach, the effect of PEG molecular weight, PVA molecular weight and alkaline pH values on water content and mechanical performance was evaluated. The used procedure permitted the theta gels to maintain swelling properties comparable to those of human cartilage, from 60% to 85%, with both polymers having the same influence. PEG MW mainly affected the hydrophilic properties, whereas the thermal properties were mostly influenced by the PVA. The shear and compression mechanical behavior of the produced materials were affected by both the polymers’ MWs. The sample obtained using PVA 125 kDa with PEG 20 kDa as a porogen appeared to be the most suitable one for cartilage disease treatment, as it had an equilibrium shear modulus in the range of 50–250 kPa, close to that of native articular cartilage, as well as optimal mechanical response under compression along the entire analyzed frequency range with a mean value of 0.12 MPa and a coefficient of friction (COF) which remained under 0.10 for all the tested sliding speeds (mm/s). Full article

The catalytic hydrogenation of the toxic and harmful p-chloronitrobenzene to produce the value-added p-chloroaniline is an essential reaction for the sustainable chemical industry. Nevertheless, ensuring satisfactory control of its chemoselectivity is a great challenge. In this work, a N/S co-doped metal-free carbon catalyst has been fabricated by using cysteine as a source of C, N, and S. The presence of calcium citrate (porogen agent) in the mixture subjected to pyrolysis provided the carbon with porosity, which permitted us to overcome the issues associated with the loss of heteroatoms during an otherwise necessary activation thermal treatment. Full characterization was carried out and the catalytic performance of the metal-free carbon material was tested in the hydrogenation reaction of p-chloronitrobenzene to selectively produce p-chloroaniline. Full selectivity was obtained but conversion was highly dependent on the introduction of S due to the synergetic effect of S and N heteroatoms. The N/S co-doped carbon (CYSCIT) exhibits a mesoporous architecture which favors mass transfer and a higher doping level, with more exposed N and S doping atoms which act as catalytic sites for the hydrogenation of p-chloronitrobenzene, resulting in enhanced catalytic performance when compared to the N-doped carbon obtained from melamine and calcium citrate (MELCIT) used as a reference. Full article

The aim of this work was the characterization of polymer microspheres obtained by the suspension polymerization of divinylbenzene (DVB) and glycidyl methacrylate (GMA), depending on the pore-forming diluents and molar ratio of monomers. The assessed properties included the chemical and porous structure, thermal stability, and sorption capacity of the obtained polymers towards methylene blue. The abovementioned characteristic was carried out for two series of copolymers with molar ratios of monomers of 1:2, 1:1 and 2:1, synthetized with toluene and a mixture of decanol and benzyl alcohol. The structure of the polymers was confirmed by FTIR and elemental analysis. The results of TGA demonstrated the main influence on thermal stability was the composition of polymers, whereas the impact of porogens was negligible. The S_BET varied in the range of 12–534 m²g⁻¹ for polymers obtained with toluene and 0–396 m²g⁻¹ with the mixture of alcohols. Toluene enhanced the formation of micro- and mesopores, while the mixture of alcohols enhanced the creation of meso- and macropores. For the polymers prepared with toluene, their effectiveness in water purification decreases in the following order: DVB-GMA 2:1 > DVB-GMA 1:1 > DVB-GMA 1:2, according to the decreasing values of porous structure parameters. In the case of a series obtained with a mixture of alcohols, such correlation was not observed. Full article