Exosome-loaded hydrogels for craniofacial bone tissue regeneration.

It is common for maladies and trauma to cause significant bone deterioration in the craniofacial bone, which can cause patients to experience complications with their appearance and their ability to function. Regarding grafting procedures' complications and disadvantages, the newly emerging field of tissue regeneration has shown promise. Tissue -engineered technologies and their applications in the craniofacial region are increasingly gaining prominence with limited postoperative risk and cost. MSCs-derived exosomes are widely applied in bone tissue engineering (BTE) to provide cell-free therapies since they not only do not cause immunological rejection in the same way that cells do, but they can also perform a cell-like role. Additionally, the hydrogel system is a family of multipurpose platforms made of cross-linked polymers with considerable water content, outstanding biocompatibility, and tunable physiochemical properties for the efficient delivery of commodities. Therefore, the promising exosome-loaded hydrogels can be designed for craniofacial bone regeneration. This review lists the packaging techniques for exosomes and hydrogel and discusses the development of a biocompatible hydrogel system and its potential for exosome continuous delivery for craniofacial bone healing.

Hierarchical Nano-Electrocatalytic Reactor for High Performance Polysulfides Redox Flow Batteries.

The aqueous polysulfides is an important Earth-abundant and multielectron redox couple to construct high capacity density and low-cost aqueous redox flow batteries (RFB) ; nevertheless, the sluggish conversion and kinetic behavior of S2-/Sx2- result in a low power density output and poor active material utilizations. Herein, we present nanoconfined self-assembled ordered hierarchical porous Co and N codoped carbon (OHP-Co/NC) as an electrocatalytic reactor to enhance the mass transfer and redox activity of aqueous polysulfides. Finite element method simulation proves that the OHP-Co/NC with interconnected macropores and mesopores exhibits an enhanced mass transfer and delivers a larger redox electrolyte utilization of 50.1% compared to 23.3% of conventional Co/NC. Notably, the OHP-Co/NC obtained at 850 °C delivers the smallest redox peak potential difference (ΔE = 99 mV). Comparison studies of in operando Raman for aqueous polysulfides in the redox electrolyte and in situ electrochemical Raman on the single OHP-Co/NC particle for the adsorbed polysulfides were carried out. And it confirms that the OHP-Co/NC-850 catalyst has a strong adsorption of S42- and can retard the strong disproportionation and hydrolysis behavior of polysulfides on the electrocatalyst interface. Therefore, the polysulfide/ferrocyanide RFB with an OHP-Co/NC-850 based membrane-electrode assembly (MEA) exhibited a high power density of 110 mW cm-2, as well as a steady capacity retention over 99.7% in 300 cycles.

Application of 3D magnetic nanocomposites: MXene-supported Fe3O4@CS nanospheres for highly efficient adsorption and separation of dyes.

Due to the presence of several hydroxyl and amino groups on the surface, chitosan (CS) has been reported to be a potential candidate to solve the pollution caused by dyes in different industrial wastewater. However, it is associated with the recycling issues. Nano-Fe3O4 has the advantages of easy magnetic separation and surface functionalization, which can improve the efficiency as well as selectivity of separation. However, its tendency for agglomeration can reduce the adsorption capacity. MXene can provide suitable support for both CS and Fe3O4 to construct new MXene@Fe3O4@CS composites. In this study, MXene@Fe3O4@CSmagnetic nanosphere was synthesized by ultrasonic self-assembly to remove Congo red (CR). Scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray photoelectron spectroscopy (XPS), and Fourier Transform Infrared (FT-IR) spectroscopy were employed to characterize the nanocomposites. According to the batch experiments, the adsorption kinetics were found to predominantly follow quasi-secondary rate kinetics. The adsorption followed Langmuir isotherm model. The adsorption process was found to be endothermic, entropy-driven, and thermodynamically spontaneous process. The adsorption capacity for CR was estimated as 620.22 mg·g-1.

A novel Zn-Al spinel-alumina composite supported gold catalyst for efficient CO oxidation.

A spinel-alumina inert oxide supported gold catalyst with high Au dispersion and excellent CO oxidation activity was developed by a deposition-precipitation method. The activation atmosphere could tune the reaction pathway by adjusting the amount of surface adsorbed water species, thus transforming the reaction intermediates from HCO3- or CO32- to COOH.

Efficient Ce-Co composite oxide decorated Au nanoparticles for catalytic oxidation of CO in the simulated atmosphere of a CO2 laser.

Gold nanoparticles have a high activity for CO oxidation, making them suitable to be used in a CO2 laser which maintains its efficiency and stability via the recombination of CO and O2 produced by the CO2 decomposition. However, the high concentration of CO2 in the working environment greatly reduces the activity of the catalyst and makes the already unstable gold nanoparticles even more so. A novel Au/Ce-Co-O x /Al2O3 gold catalyst, prepared by a deposition precipitation method in this study, displays high activity and good stability for CO oxidation in a simulated atmosphere of a CO2 laser with the feed gases containing a high concentration of CO2 up to 60 vol% but a low concentration of O2 for the stoichiometric reaction with CO. An excellent performance for CO oxidation under CO2-rich conditions could be achieved by decorating the surface of the Al2O3 support with Ce-Co composite oxides. The strong interaction between gold and the composite support, accompanied by the increase of labile lattice oxygen species and the decrease of surface basicity, led to a high CO oxidation rate and resistance towards CO2 poisoning.

Remarkable active-site dependent H2O promoting effect in CO oxidation.

The interfacial sites of supported metal catalysts are often critical in determining their performance. Single-atom catalysts (SACs), with every atom contacted to the support, can maximize the number of interfacial sites. However, it is still an open question whether the single-atom sites possess similar catalytic properties to those of the interfacial sites of nanocatalysts. Herein, we report an active-site dependent catalytic performance on supported gold single atoms and nanoparticles (NPs), where CO oxidation on the single-atom sites is dramatically promoted by the presence of H2O whereas on NPs' interfacial sites the promoting effect is much weaker. The remarkable H2O promoting effect makes the Au SAC two orders of magnitude more active than the commercial three-way catalyst. Theoretical studies reveal that the dramatic promoting effect of water on SACs originates from their unique local atomic structure and electronic properties that facilitate an efficient reaction channel of CO + OH.

Ammonia modification for flotation separation of polycarbonate and polystyrene waste plastics.

A promising method, ammonia modification, was developed for flotation separation of polycarbonate (PC) and polystyrene (PS) waste plastics. Ammonia modification has little effect on flotation behavior of PS, while it changes significantly that of PC. The PC recovery in the floated product drops from 100% to 3.17% when modification time is 13min and then rises to 100% after longer modification. The mechanism of ammonia modification was studied by contact angle, and Fourier transform infrared (FT-IR) and X-ray photoelectron spectroscopy (XPS) measurements. Contact angle of PC indicates the decline of PC recovery in the floated product is ascribed to an increase in surface wettability. FT-IR and XPS spectra suggest that ammonia modification causes chemical reactions occurred on PC surface. Flotation behavior of ammonia-modified PC and PS was investigated with respect to flotation time, frother concentration and particle sizes. Flotation separation of PC and PS waste plastics was conducted based on the flotation behavior of single plastic. PC and PS mixtures with different particle sizes are separated efficiently, implying that the technology possesses superior applicability to particle sizes of plastics. The purity of PS and PC is up to 99.53% and 98.21%, respectively, and the recovery of PS and PC is larger than 92.06%. A reliable, cheap and effective process is proposed for separation of PC and PS waste plastics.

Interfacial interactions between plastic particles in plastics flotation.

Plastics flotation used for recycling of plastic wastes receives increasing attention for its industrial application. In order to study the mechanism of plastics flotation, the interfacial interactions between plastic particles in flotation system were investigated through calculation of Lifshitz-van der Waals (LW) function, Lewis acid-base (AB) Gibbs function, and the extended Derjaguin-Landau-Verwey-Overbeek potential energy profiles. The results showed that van der Waals force between plastic particles is attraction force in flotation system. The large hydrophobic attraction, caused by the AB Gibbs function, is the dominant interparticle force. Wetting agents present significant effects on the interfacial interactions between plastic particles. It is found that adsorption of wetting agents promotes dispersion of plastic particles and decreases the floatability. Pneumatic flotation may improve the recovery and purity of separated plastics through selective adsorption of wetting agents on plastic surface. The relationships between hydrophobic attraction and surface properties were also examined. It is revealed that there exists a three-order polynomial relationship between the AB Gibbs function and Lewis base component. Our finding provides some insights into mechanism of plastics flotation.

La-doped Al2O3 supported Au nanoparticles: highly active and selective catalysts for PROX under PEMFC operation conditions.

La-doped γ-Al2O3 supported Au catalysts show high activity and selectivity for the PROX reaction under PEMFC operation conditions. The superior performance is attributed to the formation of LaAlO3, which suppresses H2 oxidation and strengthens CO adsorption on Au sites, thereby improving competitive oxidation of CO at elevated temperature.

Enhancement of acetylene hydrogenation activity over Ni-Zn bimetallic catalyst by doping with Au.

A series of modified Ni-Zn bimetallic catalysts were prepared by depositing different kinds of 4 wt% metals (Ir, Pt, Au, Cu, Ag) on the Ni-Zn-Al hydrotalcite (NZAH) and tested in the selective hydrogenation of acetylene. The activity was enhanced by 3-fold over the 4 wt% Au/NZAH, meanwhile, the yield of C2H4 was also increased more than 4 times compared with the NZAH. Characterization by means of H2-TPR, XRD, SEM, and TEM revealed that Au was highly dispersed on the catalyst, and the ternary Au-Ni-Zn alloy was formed during the H2 reduction at 500 degrees C. Doping Au in Ni-Zn bimetallic catalyst weakens the adsorption of acetylene and also hinders the coke deposition on the catalyst, which leads to the enhanced activity in acetylene hydrogenation.

Cooperativity between the halogen bond and the hydrogen bond in H3N...XY...HF complexes (X, Y=F, Cl, Br).

Ab initio calculations are used to provide information on H(3)N...XY...HF triads (X, Y=F, Cl, Br) each having a halogen bond and a hydrogen bond. The investigated triads include H(3)N...Br(2)-HF, H(3)N...Cl(2)...HF, H(3)N...BrCl...HF, H(3)N...BrF...HF, and H(3)N...ClF...HF. To understand the properties of the systems better, the corresponding dyads are also investigated. Molecular geometries, binding energies, and infrared spectra of monomers, dyads, and triads are studied at the MP2 level of theory with the 6-311++G(d,p) basis set. Because the primary aim of this study is to examine cooperative effects, particular attention is given to parameters such as cooperative energies, many-body interaction energies, and cooperativity factors. The cooperative energy ranges from -1.45 to -4.64 kcal mol(-1), the three-body interaction energy from -2.17 to -6.71 kcal mol(-1), and the cooperativity factor from 1.27 to 4.35. These results indicate significant cooperativity between the halogen and hydrogen bonds in these complexes. This cooperativity is much greater than that between hydrogen bonds. The effect of a halogen bond on a hydrogen bond is more pronounced than that of a hydrogen bond on a halogen bond.