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Biomass-derived activated carbon is a widely used electrode material for supercapacitors. One of the keys to preparing high-performance activated carbon is the selection of appropriate precursors. Daylily is a common edible herb and is widely planted in Asia. It is rich in nitrogen and phosphorus, so it can be used as a precursor of heteroatom-doped activated carbon. Herein, a daylily-derived porous carbon with a large specific surface area and high content of heteroatoms has been successfully prepared by a simple carbonization method. The as-prepared carbon materials showed a remarkable specific capacitance of 299.1 F/g at 0.5 A/g and excellent cycling stability of 99.6% after 4000 cycles at a current density of 1 A/g. Moreover, the assembled symmetric supercapacitor showed a high energy density of 21.6 Wh/kg at a power density of 598.2 W/kg in 6 M KOH electrolyte. These results demonstrate that the daylily-derived porous carbon is an excellent material for high-performance supercapacitors.

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In order to efficiently extract uranium from uranium-containing wastewater, a novel acid doped polypyrrole/carbon felt (PA-PPy/CF) electrode was prepared via a facile electrodeposition method. For this material, PA and PPy combined to form a stable chemical structure by a charge compensation mechanism. The electrochemical characterization results showed that PA-PPy can significantly accelerate the electrochemical reduction rate of uranium ions. Moreover, a double potential step technique (DPST) was applied to prevent water splitting and maintained the electrocatalytic reduction activity of the surface groups during the electrochemical adsorption process. The removal efficiency obtained by the DPST method was six times higher than that obtained by the conventional chemical adsorption. When the concentrations of uranyl nitrate were 10, 20, 50, and 100 mg/L, the removal efficiencies of uranium were 98.8%, 98.1%, 94.6%, and 93.7%, and the adsorption capacities of uranium were 164.7, 326.9, 788.5, and 1562.0 mg/g, respectively. This material also showed an excellent recycling performance and remarkable selectivity for uranium ions. This work may shed light on the development of removal system for uranium (VI).

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The development of supercapacitors with a high energy density and power density is of great importance for the promotion of energy storage technology. In this study, we designed and prepared petal-like CoMoO4 clusters combined with carbon cloth as an excellent self-standing and binder-free electrode for asymmetric supercapacitors. Due to the abundant electrochemical active sites, the promising electron conduction, and ion diffusion rate, the CoMoO4@carbon cloth (CoMoO4@CC) electrode exhibits an excellent electrochemical performance. The results show that the CoMoO4@CC material exhibits a high specific capacitance (664 F/g at a current density of 1 A/g) and an excellent cycle stability (capacitance remains at 84.0% after 1000 cycles). The assembled symmetrical supercapacitor has an energy density of 27 Wh/kg when the power density is 600 W/kg. Even at a higher power density (6022 W/kg), it still maintains a good energy density (18.4 Wh/kg).

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A three-dimensionally interconnected molybdenum trioxide (MoO3)/polypyrrole (PPy)/reduced graphene oxide (rGO) composite was synthesized via an eco-friendly three-step method. The as-obtained electrode shows a high specific capacity of 412.3 F g-1 at a current density of 0.5 A g-1 and a good cycling stability (85.1% of the initial specific capacitance after 6000 cycles at 2 A g-1 is retained), and these excellent electrochemical performances can be attributed to the unique structure, remarkable electrical conductivity, and the synergetic effects between MoO3, PPy, and rGO. Furthermore, a symmetric supercapacitor based on a MoO3/PPy/rGO electrode was assembled to investigate the practical application performance of this material. The results demonstrate a high energy density of 19.8 W h kg-1 at a power density of 301 W kg-1. These findings shine a light on the rational design of electrode materials with multicomponents for high-performance supercapacitors.

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In the present study, SWCNH-COOH and SWCNH-TETA were fabricated using single-walled carbon nanohorns (SWCNHs) via carboxylation and grafting with triethylenetetramine (TETA) for uranium (VI) ion [U(VI)] removal. The morpho-structural characterization of as-prepared adsorbing materials was performed by transmission electron microscopy, X-ray diffractometry, Raman spectroscopy, and X-ray photoelectron spectroscopy (XPS). Several parameters including the pH value of the aqueous solutions, contact time, temperature, and U(VI) concentration were used to evaluate the sorption efficiency of SWCNH-COOH and SWCNH-TETA. The Langmuir isotherm model could well represent the as-obtained adsorption isotherms, and the kinetics was successfully modeled by pseudo-second-order kinetics in the adsorption process. The maximum adsorption capacity of SWCNH-TETA was calculated as 333.13 mg/g considering the Langmuir isotherm model. Thermodynamic studies showed that adsorption proved to be a spontaneous endothermic process. Moreover, SWCNH-TETA exhibited excellent recycling performance and selective adsorption of uranium. Furthermore, the possible mechanism was investigated by XPS and density functional theory calculations, indicating that the excellent adsorption was attributed to the cooperation capability between uranium ions and nitrogen atoms in SWCNH-TETA. This efficient approach can provide a strategy for developing high-performance adsorbents for U(VI) removal from wastewater.

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Anabaena flos-aquae, a typical species of cyanobacterial bloom, was employed as a useful biosorbent for uranium removal. Batch experiments were conducted to examine the effects of different parameters on the uranium uptake amount of Anabaena flos-aquae. The maximum adsorption capacity of 196.4 mg/g was obtained under the optimized experimental conditions. The calculations of kinetic and thermodynamic results proved the adsorption process was endothermic, chemisorption, and spontaneous. The adsorption of uranium onto Anabaena flos-aquae was better defined by the Langmuir model, which indicated the process was a monolayer sorption. In addition, the characterization of the biosorbent before and after uranium sorption implied that the dominant functional groups participated in the uranium adsorption process were hydroxyl, amino, and carboxyl. In conclusion, the environmentally friendly and biocompatible characteristics of Anabaena flos-aquae suggest that it can be a promising biosorbent for uranium removal.

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Herein, the precursor polyphosphazene was synthesized by the polymerization of hexachlorocyclotriphosphazene (HCCP) and bis(4-hydroxyphenyl) sulfone (BPS). The adsorbent which was codoped with N, P and S (amidate-CS) was developed from the precursor by using the carbonization method. The images of Scanning electron microscope (SEM) and Transmission electron microscope (TEM) indicate that the amidate-CS possessed porous graphene-like carbon lamellar structure. The excellent behaviors with respect to kinetics (120 min for equilibrium) and thermodynamics (maximum removal of 290 mg/g when pH was at 6.0) revealed the outstanding performance of amidate-CS in removing U(VI), which is due to the functional groups and strong covalent bonds between heteroatoms and uranyl ions. The adsorption of amidate-CS followed the pseudo-second-order kinetic and Langmuir adsorption model. The thermodynamic parameters indicate that the process was spontaneous and endothermic. The adsorption and desorption efficiency of amidate-CS had a slight decrease after five cycles, indicating excellent regeneration performance. Overall, the amidate-CS is a prospective candidate for highly selective U(VI) removing.

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Plant research and natural product detection are of sustainable interests. Benefited by direct detection with no sample preparation, sinapine, a bioactive chemical usually found in various seeds of Brassica plants, has been unambiguously detected in radish taproot (Raphanus sativus) tissue using a liquid-assisted surface desorption atmospheric pressure chemical ionization mass spectrometry (DAPCI-MS). A methanol aqueous solution (1:1) was nebulized by a nitrogen sheath gas toward the corona discharge, resulting in charged ambient small droplets, which affected the radish tissue for desorption/ionization of analytes on the tissue surface. Thus, sinapine was directly detected and identified by tandem DAPCI-MS experiments without sample pretreatment. The typical relative standard deviation (RSD) of this method for sinapine detection was 5-8% for six measurements (S/N=3). The dynamic response range was 10(-12)-10(-7) g/cm2 for sinapine on the radish skin surface. The discovery of sinapine in radish taproot was validated by using HPLC-UV methods. The data demonstrated that DAPCI assisted by solvent enhanced the overall efficiency of the desorption/ionization process, enabling sensitive detection of bioactive compounds in plant tissue.

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PLLA microspheres were aminolyzed in hexanediamine/propanol solution to introduce free amino groups on their surface, which were further transferred into aldehyde groups by a treatment of glutaraldehyde. Chitosan-graft-lactose was then covalently coupled via Schiff base formation. Morphological variation and chitosan-graft-lactose immobilization were characterized. In vitro culture of rabbit auricular chondrocytes demonstrated that the PLLA microcarriers could effectively support the cell attachment and particularly induce cell aggregation on their surface. The formed cell aggregates/microcarriers composite showed higher viability and extracellular matrix production. Thus, the PLLA microcarriers can be potentially used as an injectable delivery system for cartilage repair.

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Poly(lactide-co-glycotide) (PLGA)/gelatin composite microspheres were prepared by an emulsion solvent evaporation technique. RGDS peptides were further immobilized under the catalyzation of water soluble carbodiimide (EDAC). Confocal laser scanning microscopy and transmission electron microscopy revealed that the gelatin was entrapped in the PLGA/gelatin microspheres with a manner of separated domains. The contents of the entrapped gelatin and immobilized RGDS peptides were quantified as 0.9 mg/20 mg and approximately 2.1 microg/20 mg microspheres by hydroxyproline analysis and bicinchoninic acid protein assay, respectively. Moreover, difference in morphology of PLGA, PLGA/gelatin and RGDS modified PLGA/gelatin (PLGA/gelatin-RGDS) microspheres was observed by scanning electron microscopy. The PLGA/gelatin and PLGA/gelatin-RGDS microspheres lost their weight rapidly in PBS, but slowly in DMEM/fetal bovine serum. Rabbit auricular chondrocytes were seeded onto the microspheres in vitro to assess their biological performance and applicability as cell carriers. Results show that amongst the PLGA, PLGA/gelatin and PLGA/gelatin-RGDS microspheres, the latter ones have the best performance in terms of chondrocyte attachment, proliferation, viability and sulfated glycosaminoglycans secretion.

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