Composite Microspheres Research Articles

Polyethylene glycol crosslinked modified chitosan/halloysite nanotube composite aerogel microspheres for efficient adsorption of melanoidin

Melanoidins are widely present in molasses wastewater and are dark-colored macromolecules that are hazardous to the environment. Currently, adsorption methods can effectively remove melanoidins from wastewater. However, existing adsorbents have shown unsatisfactory removal efficiency for melanoidins, making practical application challenging. Polyethylene glycol crosslinked modified chitosan/halloysite nanotube composite aerogel microspheres (PCAM@HNTs) were developed as a highly efficient adsorbent for melanoidins. The removal rate of PCAM@HNTs for melanoidins was 98.53 % at adsorbent dosage 0.4 mg/mL, pH 7, temperature 303 K and 450 mg/L initial melanoidins concentration, and the corresponding equilibrium adsorption capacity was 1108.49 mg/g. The analysis results indicate that the adsorption of melanoidins by PCAM@HNTs is a spontaneous and endothermic process. It fits well with pseudo-second-order kinetic models and the Freundlich isotherm equation. The adsorption of PCAM@HNT on melanoidins is primarily attributed to electrostatic and hydrogen bonding interactions. Furthermore, PCAM@HNTs exhibit excellent biocompatibility and are nonhazardous. Therefore, PCAM@HNTs proved to be an ideal adsorbent for the decolorization of molasses wastewater.

Composite or Modified Hydroxyapatite Microspheres as Drug Delivery Carrier for Bone and Tooth Tissue Engineering.

Since hydroxyapatite (HAp) is an important constituent of bone and teeth, it has excellent biocompatibility and bioactivity, good osteoconductive effects and the ability to induce bone formation as a material for bone or tooth repair and replacement. At present, widely used HAp microspheres have some characteristics, such as large specific surface area, light mass, good injection properties, good fluidity, and low aggregation ability, but they are difficult to really meet the biological and clinical needs due to their own mechanical property defects, such as low strength, brittleness, and poor plasticity. Based on the current research status of HAp microspheres, we summarize the research progress of various types of composite microspheres, including inorganic materials, natural polymer materials and synthetic polymer materials, and further analyze the advantages of HAp composite microspheres loaded with drug molecules, proteins and bioactive factors, so as to explore the development prospect of HAp composite microspheres as scaffolds for constructing sustained release systems. It provides a theoretical basis and research direction to prepare HAp composite micro-spheres with superior comprehensive properties so that they can be better applied in bone tissue regeneration and tooth regeneration engineering.

Electron transfer in MOF-derived cobalt-magnesium oxide–carbon microsphere composite catalytic ozonation of thiamphenicol

Cobalt-magnesium oxide–carbon microsphere composite (Co-MgO-CMS), Cobalt-carbon nanosheet composite (Co-CNS), and magnesium oxide–carbon nanorod composite (MgO-CNR) were synthesized by the MOFs self-sacrificing template method. And they were used as the catalysts for catalytic ozonation of thiamphenicol (20 mg/L) in water at an initial pH of 7.0. The phase of Co-MgO-CMS is mainly composed of metallic cobalt, magnesium oxide and carbon according to X-ray diffraction and transmission electron microscopy analyses. Thiamphenicol removal efficiency is enhanced through Co-MgO-CMS catalytic ozonation (75.4 %, in 6 min), compared with those in ozonation alone (39.8 %), Co-CNS catalytic ozonation (43.2 %), MgO-CNR catalytic ozonation (65.1 %) and Mg-Co binary oxide (Mg2CoOy) catalytic ozonation (69.0 %). Self-increasing of solution pH, protonated hydroxyl groups and electron transfer on metallic Co and lattice Co2+ are advantageous for the ozone decomposition into reactive oxygen species in Co-MgO-CMS catalytic ozonation. Owing to the metallic Co in Co-MgO-CMS, the electron transfer ability of Co-MgO-CMS is better than that of Mg2CoOy according to the in situ electrochemical test. Moreover, electron transfers directly from metallic Co to ozone. While protonated hydroxyl groups are the key for electron transfer on lattice Co2+. A possible degradation pathway for thiamphenicol in Co-MgO-CMS catalytic ozonation is proposed according to the detected intermediates. This work provides insight into improvement on electron transfer ability of concerted acid-base catalyst in heterogeneous catalytic ozonation.

Preparation of black phosphorus@sodium alginate microspheres with bone matrix vesicle structure via electrospraying for bone regeneration

Bone matrix vesicles are commonly acknowledged as the primary site of biomineralization in human skeletal tissue. Black phosphorus has exhibited favorable properties across various chemical and physical domains. In this investigation, a novel composite microsphere was synthesized through the amalgamation of sodium alginate (ALG) with black phosphorus nanosheets (BP) utilizing the electrospray (ES) technique. These microspheres were tailored to mimic the regulatory function of matrix vesicles (MV) upon exposure to a biomimetic mineralization fluid (SBF) during the biomineralization process. Results revealed that black phosphorus nanosheets facilitated the generation of hydroxyapatite (HA) on the microsphere surface. Live-dead assays and cell proliferation experiments showcased a cell survival rate exceeding 85 %. Moreover, wound healing assessments unveiled that M-ALG-BP microspheres exhibited superior migration capacity, with a migration rate surpassing 50 %. Furthermore, after 7 days of osteogenic induction, M-ALG-BP microspheres notably stimulated osteoblast differentiation. Particularly noteworthy, M-ALG-BP microspheres significantly enhanced osteogenic differentiation of osteoblasts and induced collagen production in vitro. Additionally, experiments involving microsphere implantation into mouse skeletal muscle demonstrated the potential for ectopic mineralization by ALG-BP microspheres. This investigation underscores the outstanding mineralization properties of ALG-BP microspheres and their promising clinical prospects in bone tissue engineering.

Nickel-cobalt alloy oxide nanoparticles wrapped by carbon black for efficient oxygen evolution electrocatalysis

The search for the simple and convenient design method of a non-precious metal oxygen evolution catalyst is still an emerging strategy today. Usually, nano-alloy oxide can enhance the catalytic activity for large specific surface area and active site, which have been widely studied for the purpose of developing active electrocatalysts for water splitting, while, nanoparticles are fundamentally less stable and prone to substantial size growth in long-term operations. Therefore, a framework of hierarchical porous composite microsphere with NiCoOx nanoparticles wrapped by Carbon Black (NiCoOx@CB) was fabricated successfully through spray-drying in this paper. Benefitting from the porous nanostructure and 0 D nano-alloy oxide active site, a remarkable OER performance with a low overpotential for 241 mV at 10 mA·cm−2 in alkaline media was exhibited. And, from the support of wrapped structure, NiCoOx@CB showed a superior durability with 90 h for nanoparticles were prevented to reunion during the reaction. Also, the heterogeneous interfaces with strong charge transfers between CB and NiCoOx nanoparticles could enhance OER performance (NiCoOx showed 265 mV at 10 mA·cm−2). The proposed method in this paper work provide a facile route to construct the porous composite microsphere with excellent OER electrocatalytic activity based on non-noble metal oxide wrapped by CB.

Structural coloration of white cotton fabrics via self-assembly of SiO2/carbon composite microspheres

Highly reflective substrate surfaces produce strong reflections of interfering and scattered light, which reduces the saturation and brightness of structural colors constructed by photonic crystals. Amorphous SiO2 photonic crystals of 250–360 nm were synthesized using the Stober method, and then synergized with strongly light-absorbing carbon nanoparticles to construct a variety of structural colors on the surface of white cotton fabrics by electrostatic self-assembly. The vividness and stability of the structural colors on the surface of black cotton fabrics were also compared. The results showed that the structural color cotton fabrics had excellent washing fastness and abrasion fastness. The microscopic morphology of SiO2 microspheres and structured color surfaces were investigated by Scanning electron microscopy (SEM). The compositional structure of SiO2 microspheres was analyzed by Fourier transform infrared spectroscopy (FTIR) and X-ray diffraction (XRD). The color quality of structured color cotton fabrics was investigated using reflectance spectra and K/S values.

Preparation and mechanism study of hydrogen bond induced enhanced composited gelatin microsphere probe

Fluorescent probes offer rapid and efficient detection of metal ions. However, their properties, including high biotoxicity and low detection limits, often limit their utility in biological systems. In this study, we used a microfluidic approach to fabricate photocrosslinked gelatin microspheres with a micropore, providing a straightforward method for loading fluorescent probes into these microspheres based on the adsorption effect and hydrogen bonding interaction. The gelatin microsphere loaded probes, GelMA/TPA-DAP and GelMA/TPA-ISO-HNO were designed and obtained. The results show that these probes exhibit obviously low biotoxicity compared to the original molecular probes TPA-DAP and TPA-ISO-HNO. Simultaneously, it is found that GelMA/TPA-DAP and GelMA/TPA-ISO-HNO have better detection sensitivity, the detection limits are 35.4 nM for Cu2+, 16.5 nM for Co2+ and 20.5 nM for Ni2+ for GelMA/TPA-DAP probe. Compared to the original TPA-DAP they are improved by 37.2 %, 26.3 % and 22.6 % respectively. The corresponding coordination constants were 10.8 × 105, 4.11×105 and 6.04×105, which is larger than homologous TPA-DAP. Similar results were also verified in the GelMA/TPA-ISO-HNO probe. The mechanism was investigated in detail by theoretical simulations and advanced spectral analysis. The density functional theory (DFT) simulations show that the probes are anchored inside the microspheres and the molecular structure is modified due to the hydrogen bonding interaction between the microsphere and the molecular probe, which makes GelMA/TPA-DAP exhibit stronger coordination capacity with metal ions than homologous TPA-DAP. In addition, the adsorption effect also provided some synergistic enhancement contribution. Meanwhile, cellular experiments have also shown that the composite microspheres can improve the biocompatibility of the probe and will provide a wider range of applications towards bioassay. This simple and effective method will provide a convenient way to improve the performance of fluorescent probes and their biological applications.

Ion‐Engineered Microcryogels via Osteogenesis‐Angiogenesis Coupling and Inflammation Reversing Augment Vascularized Bone Regeneration

AbstractNative bone inherently requires a balanced ionic microenvironment to maintain bone homeostasis. Hence, scaffolds designed for the sustained release of therapeutic ions into bone defects hold great promise for bone regeneration. Magnesium (Mg) and silicon (Si) are essential elements, which play crucial roles in the process of bone regeneration, impacting immunomodulation, angiogenesis, and osteogenesis. Herein, porous cryogel‐type organic–inorganic composite microspheres are developed as injectable microscaffolds (denoted as GMN). GMN enables sustained release of Mg/Si ions at an optimized ratio, achieving the most significant synergistic effect on vascularized bone regeneration. Various conditioned media are obtained to explore angiogenesis‐osteogenesis coupling, as well as the crosstalk between bone marrow mesenchymal stromal cells (BMSCs) and macrophages. Meanwhile, autocrine and paracrine effects simultaneously play synergistic modulating functions in determining cell fates under the guidance of Mg/Si ions and biofactors secreted by cells. Overall, the Mg/Si ion‐engineering microscaffolds create a conducive microenvironment to efficiently augment the regeneration of vascularized bone tissue in vivo, offering a versatile platform for tissue engineering.

Micron-Sized Thiol-Functional Polysilsesquioxane Microspheres with Open and Interconnected Macropores: Preparation, Characterization and Formation Mechanism.

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.

Selective adsorption and identification of penicillin G sodium in milk by molecularly imprinted polymer doped carbon dot.

A carbon dot (CD) was prepared by o-phenylenediamine and water, which showed bright yellow fluorescence under ultraviolet light irradiation (λ = 580nm), and verified good fluorescence quenching effect on penicillin G sodium (Png-Na). Using methacrylic acid as a functional monomer, ethylene glycol dimethacrylate as a crosslinker, and Png-Na as a template, a kind of composite microsphere combining CD and molecularly imprinted polymer (MIP) was synthesized by surface-initiated atomic transfer radical polymerization (SI-ATRP). For reasons ofcomparison, we also prepared MIP without CD and non-imprinted polymers (NIPs). Through static and dynamic adsorption experiments, the maximum adsorption capacity was 47.05mgg-1 and the equilibrium time was 30min. High-performance liquid chromatography (HPLC) was utilized to determine the content of Png-Na in the spiked milk samples. A sensitive, rapid, and simple method for determination of Png-Na in food samples was developed. The utilized approach enabled the quantification of Png-Na within theconcentration range 20-1000μg L-1 (with a limit of detection of 5μg L-1). The recoveries achieved were in the range 93.3-98.2%, with a relative standard deviation of 1.2-4.2%. The results demonstrated that CD@MIP possessed the capability of specific adsorption and fluorescence detection of Png-Na, enabling simultaneous detection and enrichment of Png-Na in real samples.

Preparation and characterization of silver-carbon composite semitransparent hollow microspheres for surface-enhanced Raman scattering

In this work, silver-carbon composite semitransparent hollow spheres (Ag/HCSs) have been successfully synthesized via hydrothermal carbonization (HTC) with trioctylamine (TOA) as a stabilizer and soft template. Furthermore, silver-carbon composites with core-shell structure (Ag@CSs) and carbon films loaded with silver nanoparticles composites with lamellar structure (Ag/CFs) were prepared by adjusting the amount of TOA. The Ag/HCSs were composed of a matrix of ultrathin translucent hydrothermal hollow carbon microspheres with Ag nanoclusters embedded, and numbers of Ag@CSs inside and outside of the hollow carbon microspheres. We further investigated the growth mechanism and morphology evolution, on the basis of the properties of Ag and HCSs, explored the application of the Ag/HCSs for surface-enhanced Raman scattering (SERS). SERS activity was investigated using Rhodamine 6 G (R6G) and crystal violet (CV) as the SERS probe molecules. Ag/HCSs exhibit the best SERS performance among three products. The semitranslucent carbon shell, localized surface plasmon resonances of AgNPs and the effect of charge transfer arising from oxygen-containing moieties make the Ag/HCSs to exhibit good SERS performance, which may give a little inspiration to prepare novel SERS substrates.

Biomimetic fabrication of sr-silk fibroin co-assembly hydroxyapatite based microspheres with angiogenic and osteogenic properties for bone tissue engineering

Bone defects caused by trauma, tumor resection, or developmental abnormalities are important issues in clinical practice. The vigorous development of tissue engineering technology provides new ideas and directions for regenerating bone defects. Hydroxyapatite (HAp), a bioactive ceramic, is extensively used in bone tissue engineering because of its excellent osteoinductive performance. However, its application is challenged by its single function and conventional environment-unfriendly synthesis methods. In this study, we successfully "green" synthesized sr-silk fibroin co-assembly hydroxyapatite nanoparticles (Sr-SF-HA) using silk fibroin (SF) as a biomineralized template, thus enabling it to have angiogenic activity and achieving the combination of organic and inorganic substances. Then, the rough composite microspheres loaded with Sr-SF-HA (CS/Sr-SF-HA) through electrostatic spraying technology and freeze-drying method were prepared. The CCK-8 test and live/dead cell staining showed excellent biocompatibility of CS/Sr-SF-HA. Alkaline phosphatase (ALP) staining, alizarin red staining (ARS), immunofluorescence, western blotting, and qRT-PCR test showed that CS/Sr-SF-HA activated the expression of related genes and proteins, thus inducing the osteogenic differentiation of rBMSCs. Moreover, tube formation experiments, scratch experiments, immunofluorescence, and qRT-PCR detection indicated that CS/Sr-SF-HA have good angiogenic activity. Furthermore, in vivo studies showed that the CS/Sr-SF-HA possesses excellent biocompatibility, vascular activity, as well as ectopic osteogenic ability in the subcutaneous pocket of rats. This study indicates that the construction of CS/Sr-SF-HA with angiogenic and osteogenic properties has great potential for bone tissue engineering.

Preparation of magnetic DTPA-modified chitosan composite microspheres for enhanced adsorption of Pb(II) from aqueous solution

In this study, magnetic DTPA-modified chitosan composite microspheres (MDCM) were prepared by reverse emulsion-double crosslinking method (carbodiimide followed by glutaraldehyde) for removal of Pb(II) from aqueous solution. The obtained magnetic adsorbents were characterized by FTIR, SEM, XRD, VSM, BET, and 13C NMR. The effects of the pH, contact time, initial concentration, and competitive metal cations (Na(I), Ca(II), or Mg(II)) on Pb(II) adsorption were investigated. The results revealed that MDCM exhibited high removal performance over a wide pH range and in the presence of competitive metal cations. The maximum adsorption capacity of MDCM for Pb(II) is 214.63 mg g−1 at pH 3, which is higher than most recently reported magnetic adsorbents. Adsorption kinetics and isotherms can be described by the pseudo-second-order model and Langmuir model, respectively. In addition, MDCM is easy to regenerate and can be reused five cycles with high adsorption capacity. Finally, the adsorption mechanism was further revealed by FTIR and XPS analysis. Overall, MDCM has practical application potential in removing Pb(II) from contaminated wastewater due to its high adsorption efficiency, good reusability, and convenient magnetic separation.

Efficient NiFeCr0.1/NF by incorporating chromium to boost OER catalysis

This study developed ternary NiFeCr hydroxide microsphere composites for efficient oxygen evolution reaction (OER) in alkaline water. Compared to binary NiFe composites, the ternary composites exhibited superior electrocatalytic activity. In a 1 M KOH solution, the ternary composite demonstrated a low initial potential of 1.46 V (RHE), and the overpotential is only 268 mV @ 100 mA cm−2. Charge rearrangement due to chromium oxidation helped maintain iron's low oxidation state, preserving OER activity. The redistribution of chromium particles stabilized iron and prevented its dissolution in an alkaline solution. Consequently, the optimized NiFeCr catalyst exhibits excellent stability, with a stability of 200 h at 100 mA cm−2. This study offers a novel approach to designing efficient and stable catalysts for water decomposition.

Electrospray fabrication of CL-20 composite microspheres for high-energy EFIs: Microstructure modulation and performance optimization

The utilization of high-energy explosives in Explosive Foil Initiators (EFIs) holds paramount significance. In this study, CL-20 composite microspheres were successfully prepared by electrostatic spraying technology, demonstrating narrow size distribution and high sphericity at 5% binder content. The strategy of introducing NC in GAP and F2602 effectively improved the porosity, specific surface area and apparent activation energy of CL-20 microspheres, where the increased specific surface area contributed to the narrow pulse sensibility of CL-20 microspheres. Compared to raw CL-20, these microspheres exhibited markedly improved safety properties. Comparative analysis with the HNS-IV revealed that CL-20 microspheres, with GAP/NC binder, demonstrated the minimum firing voltage of 1.10 kV and the narrow pulse initiation energy of 0.121 J, which was close to that of HNS-IV (1.08 kV and 0.117 J). However, CL-20 microspheres exhibited significantly enhanced detonation performance and output energy. The application of CL-20 microspheres in EFIs promoted the EFIs' miniaturization development.

Hemocompatible polyethylenimine-grafted poly (glycidyl methacrylate) based microspheres for effective endotoxin removal

Endotoxin (also known as lipopolysaccharide, LPS), the major component in the outer cell wall of Gram-negative bacteria, is considered to be a main cause of sepsis. To reduce the mortality of sepsis, adsorbents with positively charged surfaces like polyethylenimine (PEI) are commonly employed to adsorb endotoxins; however, there are hidden dangers in binding stability and hemocompatibility of PEI-grafted materials. Herein, poly (glycidyl methacrylate) microspheres prepared by electro-spraying are chosen as the substrate, the surface epoxy groups are utilized to chemically immobilize PEI molecules. Then, heparin coatings are introduced through electrostatic interaction to obtain composite microspheres as hemoperfusion adsorbent. As a result, the hemocompatibility of the microspheres is significantly improved after the introduction of the heparin coatings. Compared to the microspheres only grafting PEI, the hemolysis ratio has a huge decrease from 4.6% to 1.0%. The adsorption process of the composite microspheres is more consistent with Sips isotherm model with a theoretical maximum endotoxin adsorption capacity of 2659.1 EU/g in normal saline solution. And the microspheres exhibit high endotoxin clearance ratio of 81.3% in static plasma (C0 = 12.6 EU/mL, exceeding critical illness level). In vitro dynamic adsorption experiments also indicate that the microspheres remove 86.6% of endotoxin in septic plasma (C0 = 7.2 EU/mL, exceeding critical illness level) within 1 h. We hope that the composite microspheres could have good application potential as an efficiency endotoxin adsorbent in sepsis treatment.

Research Progress on the Preparation of Inorganic/Natural Materials Composite Microspheres

Microspheres are a new type of drug carrier with great potential for development and application. Natural polymers have good biocompatibility, biodegradability, and are easily dispersed in living organisms, making them suitable for preparing microspheres. Inorganic materials (mainly inorganic minerals) have excellent mechanical properties and are inexpensive and easy to obtain. Through the coupling and hybridization of natural polymers and inorganic materials, they can complement each other's advantages and synergistically enhance efficiency, resulting in many excellent physical and chemical properties. Inorganic materials/natural polymer composite microspheres can be prepared by modifying natural polymers with inorganic materials through various methods such as emulsification crosslinking, solution mixing, in-situ synthesis, extrusion, etc. The application of inorganic materials/natural polymer composite microspheres in drug delivery systems has significant sustained-release effects, is safe and non-toxic, and the cost of carrier materials is relatively low, which has certain significance for the development of new drug carriers. This article reviews the recent research on the preparation, drug loading and release properties of inorganic material/natural polymer composite microspheres, analyzes the advantages and disadvantages of commonly used preparation methods, and looks forward to the development direction of composite microspheres.

Rational design of agarose/dextran composite microspheres with tunable core–shell microstructures for chromatographic application

A new type of core-shell microsphere was prepared by a pre-crosslinking method, consisting of cross-linked agarose microspheres as the core and agarose-dextran as the shell. After optimizing the preparation process, the microspheres with a uniform particle size were obtained and characterized using cryo-scanning electron microscopy to determine their surface and cross-sectional morphology. Results from flow rate-pressure and chromatographic performance tests showed that the core-shell agarose microspheres were supported by the core microspheres and composed of composite polysaccharides, forming an interpenetrating polymer network structure as a hard shell. The core-shell agarose microspheres showed a 300.5 % increase in linear flow rate compared to composite polysaccharide microspheres prepared from shell materials and a 141.5 % increase compared to 6 % agarose microspheres. Additionally, the large pore structure of the shell combined with the fine pore structure of the core improved the material separation efficiency in the range of 0.1–2000 kDa. These findings suggest that core-shell natural polysaccharide microspheres have great potential as a separation chromatographic medium.

Optimization of process variables and characterization of mechanically agitated ceramic‐microsphere reinforced aluminium composite

AbstractThis study aims to investigate the effect of stir‐casting process parameters, including stirring speed, stirring time, and weight % of the ceramic microsphere, on the fabrication of an aluminium 6061‐ceramic microsphere composite. Experiments are conducted using a full‐factorial design approach to determine the effect of variables on mechanical properties. A field effect scanning electron microscope is used to analyze the fracture surfaces of the test specimen. Further, the results are subjected to the Anderson‐darling normality test to validate the accuracy of the model, and finally, an analysis of variance is performed to identify the most significant parameters that affect the mechanical properties. The results confirm the validity of the designed experimental model for enhancing the mechanical properties of the aluminium 6061‐ceramic microsphere composite. The optimum mechanical properties are attained for a stirring speed of 600 min−1, stirring time of 15 min, and 5 weight % of reinforcement. Furthermore, the weight percentage of the ceramic microsphere increase, the ductility of the composite decreases while its strength and hardness increase. Finally, the analysis of variance shows that all parameters significantly impact the mechanical properties of the designed composite.

Cheap and efficient strategy for photocatalytic degradation of ionic liquids by La/Ce-codoped TiO2@PAM composites.

Ionic liquids are regarded as green solvents mainly due to their non-volatile and easy regeneration and recycling properties. However, ionic liquids have negative effects on the environment and human health, especially alkyl imidazole ionic liquids are more toxic than traditional organic solutions. Studies on the toxicology, ecotoxicology, and degradation of ionic liquids are rarely found in the literature. Here, we prepared the cheap La and Ce-codoped TiO2@PAM (polyacrylamide) composite microspheres with a simple procedure for the first time to degrade three kinds of imidazole ionic liquids with high efficiency. The experimental results show that the composite La (0.25%) and Ce (0.15%)-codoped TiO2@PAM composite microspheres with calcination temperature of 450 °C had a high photocatalytic activity for 1-butyl-3-methyl imidazolium hexafluorophosphate, 1-hexyl-3-methyl imidazolium hexafluorophosphate, and 1-octyl-3-methyl imidazolium hexafluorophosphate with the concentration of 10 mg/L. The photocatalysis degradation extent of the three ionic liquids is 97.4, 91.2, and 88.5% at 90 min. This work opened a new route for the simple preparation of cheap composite microspheres in the photocatalytic degradation of ionic liquids with a high efficiency.