Large Pore Size Research Articles

Promising honeycombed cork activated carbon for high desalination performance brackish water treatment

Cork activated carbon (CAC), derived from natural cork, was successfully prepared through two steps of carbonation and activation, and used for desalinating brackish water. The CAC presents a uniform honeycomb structure composed of porous carbon nanoflakes (200–300 nm) and large specific surface area (SSA) (2680 m2 g−1), offering transport channels and a large number of adsorption sites to NaCl solution. The CAC showed excellent capacitance (116 F g−1), small internal resistance and better charge-discharge performance. Moreover, the optimized CAC showed high desalting capacity (9.44 mg g−1), charge efficiency (46.72 %), and lower energy consumption (54.19 Wh m−3) in the desalination process, superior to that of the reported biomass-based activated carbons, which can be attributed to the stable honeycomb structure, high microporous volume (0.86 cm3·g−1) and large pore size (2.43 nm). This investigation demonstrates the potential application of cork granules-based CAC electrodes in the field of desalination.

A newly NH2-UiO-66 composite functionalized by molecularly imprinted polymer for selective and rapid removal of sulfamethoxazole

Metal–organic frameworks (MOFs) are used as novel adsorption materials owing to their large surface area and tunable pore size. However, the lack of selectivity considerably limits their application. Consequently, designing functionalized MOFs with specific recognition abilities is essential for enhancing their adsorption performance. Herein, we synthesized a functionalized NH2-UiO-66 composite modified by molecularly imprinted polymers (MIP@NH2-UiO-66) via a one-step polymerization process in which NH2-UiO-66 and MIP were formed simultaneously. Results demonstrate that MIP@NH2-UiO-66 effectively recognized sulfamethoxazole (SMX) in complex matrices. The adsorption equilibrium was reached in only 30 min, and this fast SMX adsorption on MIP@NH2-UiO-66 was described by the Avrami kinetic model, which indicates a spontaneous and exothermic adsorption process. Within the pH range of 3.0–10.0, MIP@NH2-UiO-66 exhibited an optimal binding capacity for SMX, and the maximum adsorption of SMX was 68.36 mg g−1 at 25°C, which exceeded those of existing adsorption materials (< 60.10 mg g−1). Additionally, MIP@NH2-UiO-66 was regenerated for ∼17 cycles compared to less than eight cycles for the other adsorbents. MIP@NH2-UiO-66 effectively removed 90.58%–99.60% of SMX from river water, rainwater, soil, sediment, chicken, pork, and milk samples, with a relative standard deviation of less than 4.43%. The superior adsorption of SMX on MIP@NH2-UiO-66 was primarily driven by the synergistic effects of the imprinting sites, hydrogen bonding, and electrostatic forces. The one-step polymerization method substantially simplified the synthesis process and reduced the costs, which are promising factors for the synthesis of MOFs with high selectivity.

Steering Acid-base Site Distribution and Hydrophobicity of Bioresourced Bifunctional Hybrid Materials for Direct Synthesis of γ-Valerolactone from Biomass-based Furfural.

The direct production of value-added chemicals from biomass via multiple conversion processes with a sole renewable solid catalyst is promising for carbon-neutral development while challenging. Herein, a series of novel bioresourced organic-inorganic hybrid materials were synthesized from bio-based ascorbic acid (Vc), zirconium chloride (ZrCl4) and p-toluenesulfonic acid (p-TSA) through a facile solvothermal process. The as-prepared Zr-Vc-3 catalyst with Vc, ZrCl4, and p-TSA in the 1:1:0.5 molar ratio displayed outstanding performance in direct furfural-to-γ-valerolactone (GVL) transformation, giving an ultrahigh GVL yield of 76.2%, with an ideal activation energy (55.46 kJ mol-1), outperforming state-of-the-art catalysts. The superior performance of Zr-Vc-3 could be ascribed to its good reusability, relatively large pore size, suitable amount of acid-base sites, and good hydrophobicity. Mechanistic studies unveiled that Lewis acid-base sites facilitate the conversion of furfural to furfuryl alcohol and isopropyl levulinate (IPL) to 4-hydroxypentanoate via transfer hydrogenation process, while Brønsted acid sites are instrumental in the ring-opening of furfuryl alcohol to IPL and the lactonization of 4-hydroxypentanoate to GVL, overall contributing to the multi-step conversion of furfural to GVL in a single pot. This work provides a valuable reference for precisely constructing bio-based OIHMs with tailored functionalities forone-pot valorization of biomass feedstocks via tandem reactions.

Effect of Calcination Temperature in Large-Aperture Medium-Entropy Oxide (FeCoCuZnNa)O on CO2 Hydrogenation for Light Olefins

The catalytic hydrogenation of carbon dioxide is not only a way to mitigate the greenhouse effect but also provides high-value chemicals. In this work, a medium-entropy oxide catalyst (FeCoCuZnNa)O was prepared by the sol–gel method for highly active and selective hydrogenation of CO2 to value-added hydrocarbons. When reacted at 290 °C, 2.5 MPa, and 2500 mL·gcat−1·h−1, the CO2 conversion and selectivity of olefin were affected by the calcination temperature of the catalyst, and the best performances were 39% and 41.3%. The large pore size and oxygen vacancies (Ov) formed by (FeCoCuZnNa)O promote the activation of CO2 and promote the C-C coupling reaction of Fe5C2 in a hydrogenation reaction. The promoted C-C coupling reaction was related to the surface enrichment of iron species. The presence of Ov also inhibited the excessive hydrogenation reaction, further improving the selectivity of light olefins. In addition, (FeCoCuZnNa)O did not show significant deactivation within 75 h, indicating that the catalyst has strong industrial potential.

Halochromic aerogels with Ca2⁺-induced tailored porosity based on alginate/gellan integrated with Echium amoenum anthocyanins: Characterization and application for freshness monitoring of rainbow trout fillet

This study aimed to fabricate a food freshness halochromic aerogel based on alginate, gellan, and Echium amoenum anthocyanins (EA). The porosity and morphological properties of the aerogels (AG2, AG6, and AG10) were regulated by varying the concentration of CaCl2 (2, 6, 10 %). FE-SEM analysis revealed that increasing the CaCl2 content led to the formation of aerogels with enhanced overall porosity and larger pore sizes. The AG6 aerogel, characterized by a density of 23.44 ± 0.04 mg/cm³, a porosity of 91.66 ± 0.06%, and an average pore size of 306.93 ± 122.89 μm, was identified as the optimal support for the incorporation of the EA pigment. FT-IR analysis verified the formation of hydrogen bonds between the AG6 aerogel and EA molecules. Incorporating anthocyanin increased the crystallinity and thermal stability of the aerogel, as evidenced by XRD and DSC analyses. The AG6EA aerogel displayed a color shift from red to yellow over a pH range of 2–12. The AG6EA aerogel demonstrated high sensitivity to ammonia vapor and proper color stability and reversibility. The AG6EA aerogel color transitioned from purple to blue and then green through rainbow trout storage, correlating with changes in pH, total volatile basic nitrogen (TVB-N), and total viable microbial count (TVC and TPC) of the fish samples. This research extends a new insight to develop cutting-edge, susceptible, and accurate pH indicators capable of quality assessment of protein-based food products.

Water Sorption on Isoreticular CPO-27-Type MOFs: From Discrete Sorption Sites to Water-Bridge-Mediated Pore Condensation

Pore engineering is commonly used to alter the properties of metal–organic frameworks. This is achieved by incorporating different linker molecules (L) into the structure, generating isoreticular frameworks. CPO-27, also named MOF-74, is a prototypical material for this approach, offering the potential to modify the size of its one-dimensional pore channels and the hydrophobicity of pore walls using various linker ligands during synthesis. Thermal activation of these materials yields accessible open metal sites (i.e., under-coordinated metal centers) at the pore walls, thus acting as strong primary binding sites for guest molecules, including water. We study the effect of the pore size and linker hydrophobicity within a series of Ni2+-based isoreticular frameworks (i.e., Ni2L, L = dhtp, dhip, dondc, bpp, bpm, tpp), analyzing their water sorption behavior and the water interactions in the confined pore space. For this purpose, we apply water vapor sorption analysis and Fourier transform infrared spectroscopy. In addition, defect degrees of all compounds are determined by thermogravimetric analysis and solution 1H nuclear magnetic resonance spectroscopy. We find that larger defect degrees affect the preferential sorption sites in Ni2dhtp, while no such indication is found for the other materials in our study. Instead, strong evidence is found for the formation of water bridges/chains between coordinating water molecules, as previously observed for hydrophobic porous carbons and mesoporous silica. This suggests similar sorption energies for additional water molecules in materials with larger pore sizes after saturation of the primary binding sites, resulting in more bulk-like water arrangements. Consequently, the sorption mechanism is driven by classical pore condensation through H-bonding anchor sites instead of sorption at discrete sites.

Pore-expanded phosphate-functionalized mesoporous silica microsphere composites: One-pot synthesis and application for removing uranium from water

This study focused on the development of mesoporous silica microspheres with controllable mesopores for the efficient removal of uranium from nuclear waste. Utilizing n-dodecylamine as a structure-directing agent and di(2-ethylhexyl)phosphoric acid (HDEHP) as a co-templating agent, we achieved the synthesis of large silica microspheres (10–100 µm) with uniform mesopores. The incorporated HDEHP served as both a swelling agent and a phosphate-functionalization reagent, facilitating the adsorption of bulky organic uranium sequestration agents. Our approach circumvented the need for high-temperature calcination and extensive use of organic solvents, making it an environmentally friendly and cost-effective alternative. The synthesized silica microspheres demonstrated superior adsorption capacity for uranyl ions, which was attributed to their large pore size and high surface area. The adsorption isotherms, well-fitted to the Langmuir model, suggested a maximum adsorption capacity of 136 mg g−1 at pH 4.0 with a uranium concentration of 100 mg L−1 to maintain a stable soluble phase. However, many studies have often overlooked solid-phase formation due to hydrolysis, which can overestimate the adsorption capacity. In addition, the particle size range enabled easy recovery through low-g-force centrifugation or natural sedimentation. This study highlighted the potential of phosphate-functionalized mesoporous silica microspheres as effective and reusable uranium adsorbents, thereby addressing both energy sustainability and environmental safety. The practical applications of these materials in uranium recovery and nuclear waste management underscore their importance in the nuclear industry.

Efficacy of a saline wash plus vancomycin/tobramycin-doped PVA composite (PVA-VAN/TOB-P) in a mouse pouch infection model implanted with 3D-printed porous titanium cylinders.

The efficacy of saline irrigation for treatment of implant-associated infections is limited in the presence of porous metallic implants. This study evaluated the therapeutic efficacy of antibiotic doped bioceramic (vancomycin/tobramycin-doped polyvinyl alcohol composite (PVA-VAN/TOB-P)) after saline wash in a mouse infection model implanted with titanium cylinders. Air pouches created in female BalBc mice by subcutaneous injection of air. In the first of two independent studies, pouches were implanted with titanium cylinders (400, 700, and 100 µm pore sizes) and inoculated with Staphylococcus aureus (1 × 103 or 1 × 106 colony-forming units (CFU)/pouch) to establish infection and biofilm formation. Mice were killed after one week for microbiological analysis. In the second study, pouches were implanted with 400 µm titanium cylinders and inoculated with S. aureus (1 × 103 or 1 × 106 CFU/pouch). Four groups were tested: 1) no bacteria; 2) bacteria without saline wash; 3) saline wash only; and 4) saline wash plus PVA-VAN/TOB-P. After seven days, the pouches were opened and washed with saline alone, or had an additional injection of PVA-VAN/TOB-P. Mice were killed 14 days after pouch wash. The first part of the study showed that low-grade infection was more significant in 400 µm cylinders than cylinders with larger pore sizes (p < 0.05). The second part of the study showed that saline wash alone was ineffective in eradicating both low- and high-grade infections. Saline plus PVA-VAN/TOB-P eradicated the titanium cylinder-associated infections, as manifested by negative cultures of the washouts and supported by scanning electron microscopy and histology. Porous titanium cylinders were vulnerable to bacterial infection and biofilm formation that could not be treated by saline irrigation alone. Application of PVA-VAN/TOB-P directly into the surgical site alone or after saline wash represents a feasible approach for prevention and/or treatment of porous implant-related infections.

Deposition of Imidazole into Mesoporous Zirconium Metal-Organic Framework for Iodine Capture.

Efficient capture of radioiodine is essential for the protection of the ecological environment and the sustainable development of nuclear energy generation. Metal-organic frameworks (MOFs) and their derivatives provide alternative potential for overcoming the limitations of traditional iodine adsorbents. Herein this work, imidazole (Im) is dispersed into a robust mesoporous zirconium MOF PCN-222 by the heat deposition method, forming a high-uniformity composite Im@PCN-222. The large pore size and marked chemical resistance skeleton of PCN-222 allow the incorporation of Im to reach 43 wt % while surviving the chemical corrosion of activated Im. The nearly saturated loading of Im significantly benefits the sorption capability toward iodine and gives rise to an exceptional adsorption capacity of 10.04 g g-1 and excellent recyclability. This value is higher than that of most of the MOFs and their derivatives. Further, Im was also successfully deposited onto the PCN-222 functionalized porous Al2O3 ceramic filtration membrane, which endowed the hybrid membrane with efficient iodine sorption and separation properties. This work highlights a new strategy for the fabrication of the MOF-based radioiodine adsorption composite as well as MOF composite-based filters.

Powering Hydrogen Evolution Reaction by Precise Control Over A Cu‐Ni Bimetallic Electrocatalyst

ABSTRACTPrecious metals are effective catalysts for the hydrogen evolution reaction, but their high cost with complicated operation steps drives people to search for non–noble‐metal alternatives. Building rational design concept for efficient electrocatalyst relies on the capability to control the structure and composition. Herein, a Ni/Cu bimetallic mesoporous MOFs with 4,4′,4″‐(1,3,5‐triazine‐2,4,6‐triyl)tribenzoic acid as the robust ligand has been assembled via a one‐step solvothermal method. Due to the extensive conjugate plane and high nitrogen content, the catalyst possesses large pore size of 17 nm and fast electron transfer rate, which favors hydrogen bubble overflow and exposes more active sites to solid–liquid interfaces. The bimetallic interaction between highly conductive Cu ions and Ni ions allows it to improve charge migration and realize excellent conductivity. The functionalized electrode requires an overpotential of 132 mV to achieve 10 mA current density with a small Tafel slope (87.7 mV·dec−1) and continuous electrolysis for 24 h.

Green self-templated synthesis of P-doped mesoporous carbon from dual sodium salts with improved average pore size for capacitive deionization

Mesoporous carbon materials hold significant potential in capacitive deionization (CDI) technology owing to expansive accessible surface area, more adaptable pore structure, excellent conductivity properties and effective surface modification and functionalization. While templating is a common method for synthesizing mesoporous carbons, the commonly used hard and soft templating approaches among them suffer from the challenges of expensive precursors and templating agents, complex procedures, secondary contaminants and difficulties in template removal. In contrast, the self-templating method not only circumvents the traditional template removal or combustion steps but also eliminates the use of organic solvents and hazardous chemicals, thus minimizing environmental impact. In this paper, we have successfully synthesized phosphorus-doped mesoporous carbon with a large average pore size (paver) using a green and convenient self-templating method employing dual sodium salts of sodium alginate (SA) and sodium phytate (SP). Compared to single SA (6.76 nm) or SP (3.74 nm) self-templated carbonization, the average pore size of carbon materials obtained from dual self-templated carbonization with a proportional mixture (12.97 nm) is significantly improved. The larger average pore size provides a greater surface area for electrode-electrolyte interactions, allowing for easier access and faster diffusion of ions into the pores, thereby enhancing the electrochemical and capacitive deionization properties of the material. The resulting material demonstrates promising electrochemical and desalination performance as evidenced by possessing a specific capacitance of 175.8 A/g and an adsorption capacity of 19.65 mg/g, underlining its potential for application in capacitive deionization utilizing mesoporous carbon materials with large average pore size.

Durability of a Metakaolin-Incorporated Cement-Based Grouting Material in High Geothermal Tunnels.

To improve the durability of cement-based grout in high geothermal tunnel grouting projects, metakaolin was incorporated to replace 8% of the cement. The permeability, chloride penetration, and sulfate and carbonate erosion tests were carried out on the grout cured at varying temperatures (20, 30, 40, 50, and 60 °C). It was shown that with the increase in curing temperature, the impermeability and resistance to chloride penetration initially increased and then decreased, reaching the highest values at 40 °C. Furthermore, the incorporation of metakaolin into grout enhanced the impermeability by 11.11-38.91% and resistance to chloride penetration by 12.23-12.77%. As attacked by sulfate, the surface spalling of the specimen was more obvious with the increase in the curing temperature and immersion time. Conversely, the appearance remained almost unchanged under carbonate erosion. As immersion time increased, both the antisulfate and anticarbonate erosion coefficients declined. The effect of curing temperature on erosion resistance was assessed via the relative antierosion coefficient. When immersed in sulfate, the coefficient achieved the highest value of 1.08 as cured at 30 °C, and in carbonate, the coefficient reached a maximum of 0.99 as cured at 40 °C. Through scanning electron microscopy and binarized images, it was verified that gypsum and ettringite were formed during sulfate attack, leading to volume expansion and cracking, consequently reducing the strength. Meanwhile, in the case of carbonate erosion, calcium hydroxide (CH) and calcium silicate hydrate gel (C-S-H) were dissolved and degraded, resulting in a large number and size of pores in the grout. The research results have certain theoretical significances and reference values for the application of cement-based grouting materials in high geothermal environments.

Mineral formation and element migration in fractures and pores of hydrogenetic ferromanganese nodules

Ferromanganese (Fe-Mn) nodules composed of nano-sized Fe-Mn (oxyhydr)oxides are significant mineral resources rich in multiple critical metals (e.g., Co, Ni, Cu, and REY). The ubiquitous high porosity, large pore size, and pore connectivity in hydrogenetic nodules enable the constant influx of seawater and/or porewater driving widespread diagenetic processes (i.e., mineral dissolution and recrystallization) in the abundant fractures and pores. These diagenetic processes are critical to understanding the migration, partitioning, and distribution of the critical metals, but remain unclear yet. In this study, high-resolution in-situ analyses were conducted to investigate the mineralogical and geochemical characteristics of diagenetic precipitates in fractures and pores of a hydrogenetic Fe-Mn nodule (MP5D33) from the central Pacific. Both oxic and suboxic processes were found in the fracture. The oxidized diagenetic products exhibit geochemical and mineralogical characteristics similar to those of hydrogenetic precipitates (e.g., vernadite), while the suboxic diagenetic processes primarily produced large-size 10 Å phyllomanganate. The diagenetic conditions within this studied fracture gradually shifted from oxic to suboxic, causing changes in the contents of multiple critical metals. The minerals in pores are mainly composed of 10 Å phyllomanganate that crystallized forms through heterogeneous nucleation on small-size vernadite in a suboxic environment. Additionally, minor todorokite likely transformed from 10 Å phyllomanganate undergoing long-term diagenesis. These findings shed some insights into the diagenetic process in the interior fractures and/or pores of Fe-Mn nodules and enhance the understanding of the migration of critical elements associated with Fe-Mn (oxyhydr)oxides during diagenesis in Fe-Mn deposits.

Synergistic effects of deep eutectic solvents on the morphology and performance of polysulfone ultrafiltration membranes

This study investigates the synthesis of flat sheet asymmetric Polysulfone (PSF) membranes using the Non-Solvent Induced Phase Separation (NIPS) method, enhanced by incorporating Deep Eutectic Solvents (DES) composed of Choline Chloride (ChCl) and DL-Malic Acid (MA). The research explores the individual and combined effects of ChCl and MA on membrane morphology and performance. Comprehensive characterization techniques, including Scanning Electron Microscopy (SEM), Fourier Transform Infrared Spectroscopy-Universal Attenuated Total Reflectance (FTIR-UATR), and Atomic Force Microscopy (AFM), were employed to analyze the structural and surface properties of the membranes. Key performance metrics such as Pure Water Permeability (PWP), protein and dye rejection, fouling behavior, porosity, surface hydrophilicity, and mechanical strength were evaluated. Results demonstrated that integrating DES into the PSF matrix significantly improved membrane properties. The 3% DES membrane exhibited the highest Pure Water Permeability (PWP) of 186.82 L/m2h/bar, the lowest water contact angle of 68.8°, and optimal balance in surface roughness parameters, leading to superior antifouling properties with high flux recovery ratio (FRR) and balanced reversible (Rr) and irreversible fouling (Rir) components. The ChCl (HBA) membrane displayed a notable PWP of 121.62 L/m2h/bar, large pore sizes (42.72 nm), and moderate surface roughness (Ra of 3.32 nm). In contrast, the MA (HBD) membrane demonstrated the highest hydrophilicity with the lowest contact angle (70.7°) and a compact, robust structure, despite its smallest pore sizes and lack of permeability. The findings underscore the synergistic effect of DES formation in the membrane, improving overall performance for ultrafiltration applications. This study provides valuable insights into the distinct roles of ChCl as an HBA and MA as an HBD in DES-modified PSF membranes, revealing their individual contributions and the importance of optimizing DES components and concentrations for specific filtration applications.

Elimination of hydrogen bonds in cellulose enables high-performance disordered carbon anode in sodium-ion batteries

Pre-oxidation remains an advantageous method to regulate the cross-linking structure of cellulose to prepare an increasingly disordered hard carbon applied in sodium-ion batteries. However, it is ambiguous how the introduction of oxygen affects the changes in the molecular structure of cellulose as well as the micro-structure of hard carbon. We herein systematically investigate the effect of air pre-oxidation on the crystallinity and cross-linking structure of cellulose macro-molecules by controlling the degree of oxidation. The findings indicate that the introduction of air can break the hydrogen bonding network of cellulose in advance and release a large number of reactive hydroxyl groups on the surface to be oxidized to form ether and ester cross-linking bonds. Ether bonds can transversely cross-link and extend the carbon layer and the bent carbon layers enclose a well-developed connective pore structure. Additionally, the breakage of oxygen-containing functional groups leads to the escape of large amounts of oxygen-containing gases to etch out more open pore structures with large pore sizes. Benefiting from these advantages, the prepared hard carbon possesses a specific capacity of 335 mAh g−1 and 89 % of initial coulombic efficiency at 30 mA g−1 by pre-oxidating at 300 °C for 12 h.

Improved Therapeutic Efficacy: Liposome-Coated Mesoporous Silica Nanoparticles Delivering Thymoquinone to MCF-7 Cells.

Breast cancer remains a significant global health challenge, with thymoquinone showing promise as a therapeutic agent, but hindered by poor solubility. This study aimed to enhance TQ delivery to MCF-7 breast cancer cells using mesitylene- mesoporous silica nanoparticles coated with liposomes, designed for controlled drug release. Nanoparticles were synthesized using the sol-gel method and coated with phosphatidylserine- cholesterol liposomes. Different nanocharacterization techniques and in vitro assays were employed to assess the drug release kinetics, cellular uptake, cytotoxicity, and apoptosis. The nanoparticles exhibited favorable properties, including a large pore size of 3.6 nm, a surface area of 248.96 m2/g, and a hydrodynamic size of 171.571 ± 8.342 nm with a polydispersity index of 0.182 ± 0.017, indicating uniformity and stability. The successful lipid bilayer coating was confirmed by a zeta potential shift from +6.25 mV to -5.65 mV. The coated nanoparticles demonstrated a slow and sustained drug release profile, with cellular uptake of FITC-formulated nanoparticles being approximately 5-fold higher than free FITC (P < 0.0001). Cytotoxicity assays revealed a significant reduction in cell viability (P < 0.0001), reaching an IC50 value of 25 μM at 48 hours. Apoptosis rates were significantly higher in cells treated with the formulated TQ compared to the free drug and control at both 24 and 48 hours (P < 0.0001). This nanoformulation significantly enhanced TQ delivery, offering a promising strategy for targeted breast cancer therapy. Further preclinical studies are recommended to advance this approach in cancer treatment.

Purification Processes for Generating Cationic Lignin-Acrylamide Polymers.

Purification is an essential step in many polymerization processes for fabricating highly pure polymers. This study considered various purification methods for purifying the product of lignin, acrylamide (AM), and diallyl dimethylammonium chloride (DADMAC) copolymerization reactions at a laboratory scale. The charge density, yield, molecular weight, and solubility analyses confirmed that ethanol extraction and membrane filtration were the most effective processes for producing lignin-p(AM)-p(DADMAC). The 1H NMR analysis revealed that the membrane dialysis effectively removed unreacted AM and DADMAC monomers from the reaction medium. The produced samples of the ethanol-extraction and dialysis processes had higher solubility and yield compared to the product of the acidification process. Thermogravimetric studies confirmed that the ethanol-extracted and dialyzed samples had a degradation temperature (220 °C) higher than that of the acidified samples (160 °C). The rheological studies confirmed that the viscosities of the polymer solutions were influenced more by the solubility than by the molecular weight of the generated polymers within the molecular weight range examined in this study. The flocculation studies confirmed that the ethanol-extracted and dialyzed polymers were more effective flocculants than the acidified samples for the particles of a kaolinite suspension. Based on the above results, membrane filtration with a larger pore size could be an environmentally friendly method for effectively purifying lignin-p(AM)-p(DADMAC).

Strontium ranelate-loaded human hair keratin-hyaluronic acid hydrogel accelerates wound repair with anti-inflammatory and antioxidant properties

Inflammation and reactive oxygen species (ROS) production often accompany the repair of severe skin wounds, and the management of wounds has always been a clinical challenge, so the design of a hydrogel wound dressing with antioxidant and anti-inflammatory properties is of significant importance. This work incorporated strontium ranelate (SrR) into the keratin/hyaluronic acid (K/HA) hydrogel, which could scavenge ROS and reduce inflammation. The optimized hydrogel exhibits large pore size (217.2 μm), high porosity (57 %), high swelling rate (1759.52 %), and an elastic modulus (3.41 kPa). In the in vitro study, incorporating SrR into hydrogel effectively inhibited oxidative damage in mouse fibroblasts (L929) and improved anti-inflammatory effect in RAW264.7 cells stimulated by lipopolysaccharide. The in vivo study showed that, compared with the control group, the expression of ROS, IL-6 and TNF - α in the K/HA/0.5 mM SrR group were significantly reduced to 31.6 %, 39.7 % and 61.1 %, respectively. The in vivo evaluation in a full-thickness wound defect model demonstrated that K/HA/0.5 mM SrR hydrogel promotes wound healing by attenuating ROS levels, reducing inflammation, and promoting microangiogenesis. In summary, the excellent ROS scavenging and anti-inflammatory properties of SrR make the K/HA/SrR hydrogel a promising and effective strategy for wound healing.

Dissecting the effect of substrate on polyamide reverse osmosis membranes via regulating substrate pore size by drying shrinkage

Several studies have proved that the substrate significantly influences the chemical properties of reverse osmosis (RO) membranes, whereas the underlying mechanisms remain elusive. Herein, we adjusted the substrate pore size from 8.6 nm to 4.4 nm by drying shrinkage, ensuring the substrate's chemical properties remained consistent. Interestingly, we observed that an intermediate pore size (7.4 nm) of the substrate resulted in the highest exotherm, with the interfacial temperature rising to 26.8 °C, thus showing that larger pore sizes do not necessarily result in more pronounced exothermic interfacial polymerization (IP) reactions. Through multiscale simulations and various characterization techniques, we found that the IP reaction is governed by two competing effects: (1) the storage capacity of MPD, which provides the reactive monomers; and (2) the water content, which absorbs the heat in the IP reaction. Balancing these two competing factors contributes to enhancing the diffusion of MPD, thereby promoting the progression of the IP reaction. This work revealed a new mechanism through which the substrate affects RO membrane formation.

Hierarchical materials with interconnected pores from capillary suspensions for bone tissue engineering

AbstractThe increasing demand for bone grafts due to the aging population has opened new opportunities for the manufacture of porous ceramics to assist in bone reconstruction. In our study, we investigate a new, promising method to manufacture hierarchically porous structures in a straightforward and tunable way. It consists of combining the novel technology of capillary suspensions, formed by mixing solid particles and two immiscible liquids, one less than 5 vol%, with freeze casting. We have successfully achieved alumina and beta‐tricalcium phosphate (β‐TCP) materials with both &lt;2 µm and 20–50 µm as the smallest and largest pore sizes, respectively. The microstructure exhibits fully open pores and high levels of porosity (&gt;60%). The capillary suspensions’ rheological behavior indicates that silica nano‐suspensions as a secondary fluid creates a stronger internal particle network than sucrose for the alumina system. Conversely, the opposite was observed with the β‐TCP system. These differences were attributed to the change in affinity between the secondary fluids and the solid loading. In our study, both systems have served to deepen the knowledge about the new area of capillary suspensions and proved their use in hierarchical porous scaffolds for bone tissue engineering.