Highly Efficient Adsorption of Pb(II) by Functionalized Humic Acid: Molecular Experiment and Theoretical Calculation.

Environmental pollution has been widely considered by researchers, especially the heavy metals damage to the human and ecological environment is irreversible. Adsorption is an important method to remove heavy metal ions from the environment. In this paper, humic acid (HA) was functionalized by the improved Hummers method, and its adsorption capacity for Pb(II) was studied. The results of scanning electron microscope (SEM), X-ray diffraction (XRD), Roman, and Brunauer-Emmett-Teller (BET) showed that the thickness of irregular particles decreases to a layered structure during the transformation process. In addition, X-ray photoelectron spectroscopic (XPS) and Fourier transform infrared spectra (FT-IR) spectra showed that the surface of oxidized-biochar (OBC) was rich in reactive oxygen species, which was conducive to the formation of coordination bonds with Pb(II). Further adsorption experiments showed that it was a spontaneous monolayer chemisorption. The results of the DFT calculation showed that -COOH had the lowest adsorption energy for Pb(II), and it was easier to form stable chemical bonds than -OH, -C=O, and -C-O-C-. Because those oxygen-containing functional groups not only can promote electrostatic attraction but also are more favorable for forming a covalent bond with Pb(II). This study had guiding significance for the deep modification and application of weathered coal as a heavy metal ion adsorbent or cation exchanger.

Structure-Property Relationship, Glass Transition, and Crystallization Behaviors of Conjugated Polymers.

Conjugated polymers have gained considerable interest due to their unique structures and promising applications in areas such as optoelectronics, photovoltaics, and flexible electronics. This review focuses on the structure-property relationship, glass transition, and crystallization behaviors of conjugated polymers. Understanding the relationship between the molecular structure of conjugated polymers and their properties is essential for optimizing their performance. The glass transition temperature (Tg) plays a key role in determining the processability and application of conjugated polymers. We discuss the mechanisms underlying the glass transition phenomenon and explore how side-chain interaction affects Tg. The crystallization behavior of conjugated polymers significantly impacts their mechanical and electrical properties. We investigate the nucleation and growth processes, as well as the factors that influence the crystallization process. The development of the three generations of conjugated polymers in controlling the crystalline structure and enhancing polymer ordering is also discussed. This review highlights advanced characterization techniques such as X-ray diffraction, atomic force microscopy, and thermal analysis, which provide insights into molecular ordering and polymer-crystal interfaces. This review provides an insight of the structure-property relationship, glass transition, and crystallization behaviors of conjugated polymers. It serves as a foundation for further research and development of conjugated polymer-based materials with enhanced properties and performance.

High-efficiency adsorption of Cr(VI) and RhB by hierarchical porous carbon prepared from coal gangue.

Coal gangue (CG) is one of the largest industrial solid wastes in the world produced during the process of coal mining. The accumulation of CG is easy to cause ion leakage, which is harmful to the environment and human body. The recovery and utilization of CG are imminent. In the process, a hierarchical porous carbon (HPC) adsorbent with excellent adsorption property for Cr(VI) and rhodamine B (RhB), was prepared from CG by a two-step method and characterized by SEM, TEM, XRD, XPS, TPD and BET. The results revealed that the specific surface area of HPC is up to 2012.7 m2 g-1, and its adsorption capacities for Cr(VI) and RhB are reached 320.51 and 3086.42 mg g-1. The adsorption mechanism of RhB was the synergetic effect of physics and chemistry. While XPS results suggested that hierarchical porous carbons (HPCs) only have a chemisorption effect on Cr(VI). This study provided an idea for the preparation of HPCs from CG to remove inorganic and organic pollutants such as heavy metal Cr(VI) and RhB in water.

Synthesis of NiFeAl LDHs from electroplating sludge and Their excellent supercapacitor performance.

This work demonstrated that electroplating sludges (EPS) of specific composition may be used for the synthesis of layered double hydroxide (LDH) materials for energy applications after appropriate treatment. The unique composition and structure of EPS render it with good electrochemical energy storage performance. The EPS containing Ni, Fe, and Al was dissolved by acid and added with urea precipitator. The LDH material was prepared by a facile hydrothermal method. The increase of urea in a certain range is conducive to the formation of intact LDH. However excessive urea levels promoted the transformation from LDH to Ni(HCO3)2. Various active Ni bridged by N in ‒O‒CN promoted electron transfer, ‒O‒CN content in LDHs was proportional to the urea amount. The prepared LDHs exhibited a specific capacitance of 1652.20 F g-1 at 0.5 A g-1, and the value remained at 766.69 F g-1 after 1000 cycles. The prepared LDH has excellent supercapacitor performance, which is closely related to its structure. Therefore, the proposed recycling strategy of EPS resources can be used to prepare LDH supercapacitors, paving the way for new applications of EPS in the field of energy storage.

Pt-Bi decorated nanoporous gold for high performance direct glucose fuel cell.

Binary PtBi decorated nanoporous gold (NPG-PtBi) electrocatalyst is specially designed and prepared for the anode in direct glucose fuel cells (DGFCs). By using electroless and electrochemical plating methods, a dense Pt layer and scattered Bi particles are sequentially coated on NPG. A simple DGFC with NPG-PtBi as anode and commercial Pt/C as cathode is constructed and operated to study the effect of operating temperatures and concentrations of glucose and NaOH. With an anode noble metal loading of only 0.45 mg cm-2 (Au 0.3 mg and Pt 0.15 mg), an open circuit voltage (OCV) of 0.9 V is obtained with a maximum power density of 8 mW cm-2. Furthermore, the maximum gravimetric power density of NPG-PtBi is 18 mW mg-1, about 4.5 times higher than that of commercial Pt/C.

Ultrathin dendritic Pt3Cu triangular pyramid caps with enhanced electrocatalytic activity.

Here we report on the synthesis of novel dendritic Pt3Cu triangular pyramid caps via a solvothermal coreduction method. These caps had three-dimensional caved structures with ultrathin branches, as evidenced by high-resolution transmission electron microscopy (HRTEM) and HAADF-STEM characterization. Tuning the reduction kinetics of two metal precursors by an iodide ion was believed to be the key for the formation of an alloyed nanostructure. Electro-oxidation of methanol and formic acid showed dramatically improved electrocatalytic activities and poison-tolerance for these nanoalloys as compared to commercial Pt/C catalysts, which was attributed to their unique open porous structure with interconnected network, ultrahigh surface areas, as well as synergetic effect of the two metallic components.

One-pot hydrothermal synthesis of Mn3O4 nanorods grown on Ni foam for high performance supercapacitor applications.

Mn3O4/Ni foam composites were synthesized by a one-step hydrothermal method in an aqueous solution containing only Mn(NO3)2 and C6H12N4. It was found that Mn3O4 nanorods with lengths of 2 to 3 µm and diameters of 100 nm distributed on Ni foam homogeneously. Detailed reaction time-dependent morphological and component evolution was studied to understand the growth process of Mn3O4 nanorods. As cathode material for supercapacitors, Mn3O4 nanorods/composite exhibited superior supercapacitor performances with high specific capacitance (263 F · g-1 at 1A · g-1), which was more than 10 times higher than that of the Mn3O4/Ni plate. The enhanced supercapacitor performance was due to the porous architecture of the Ni foam which provides fast ion and electron transfer, large reaction surface area, and good conductivity.

Controllable synthesis of MnO2/polyaniline nanocomposite and its electrochemical capacitive property.

Polyaniline (PANI) and MnO2/PANI composites are simply fabricated by one-step interfacial polymerization. The morphologies and components of MnO2/PANI composites are modulated by changing the pH of the solution. Formation procedure and capacitive property of the products are investigated by XRD, FTIR, TEM, and electrochemical techniques. We demonstrate that MnO2 as an intermedia material plays a key role in the formation of sample structures. The MnO2/PANI composites exhibit good cycling stability as well as a high capacitance close to 207 F g-1. Samples fabricated with the facile one-step method are also expected to be adopted in other field such as catalysis, lithium ion battery, and biosensor.

Direct N(2)H(4)/H(2)O(2) fuel cells powered by nanoporous gold leaves.

Dealloyed nanoporous gold leaves (NPGLs) are found to exhibit high electrocatalytic properties toward both hydrazine (N(2)H(4)) oxidation and hydrogen peroxide (H(2)O(2)) reduction. This observation allows the implementation of a direct hydrazine-hydrogen peroxide fuel cell (DHHPFC) based on these novel porous membrane catalysts. The effects of fuel and oxidizer flow rate, concentration and cell temperature on the performance of DHHPFC are systematically investigated. With a loading of ~0.1 mg cm(-2) Au on each side, an open circuit voltage (OCV) of 1.2 V is obtained at 80°C with a maximum power density 195 mW cm(-2), which is 22 times higher than that of commercial Pt/C electrocatalyst at the same noble metal loading. NPGLs thus hold great potential as effective and stable electrocatalysts for DHHPFCs.

Enzyme-nanoporous gold biocomposite: excellent biocatalyst with improved biocatalytic performance and stability.

BACKGROUND: Applications involving biomolecules, such as enzymes, antibodies, and other proteins as well as whole cells, are often hampered by their unstable nature at extremely high temperature and in organic solvents. METHODOLOGY/PRINCIPAL FINDINGS: We constructed enzyme-NPG biocomposites by assembling various enzymes onto the surface of nanoporous gold (NPG), which showed much enhanced biocatalytic performance and stability. Various enzymes with different molecular sizes were successfully tethered onto NPG, and the loadings were 3.6, 3.1 and 0.8 mg g(-1) for lipase, catalase and horseradish peroxidase, respectively. The enzyme-NPG biocomposites exhibited remarkable catalytic activities which were fully comparable to those of free enzymes. They also presented enhanced stability, with 74, 78 and 53% of enzymatic activity retained after 20 successive batch reactions. Moreover, these novel biocomposites possessed significantly enhanced reaction durability under various thermal and in organic solvent systems. In a sample transesterification reaction, a high conversion rate was readily achieved by using the lipase-NPG biocomposite. CONCLUSION/SIGNIFICANCE: These nano-biocomposite materials hold great potential in applications such as biosensing, molecular electronics, catalysis, and controlled delivery.

Pt-decorated nanoporous gold for glucose electrooxidation in neutral and alkaline solutions.

Exploiting electrocatalysts with high activity for glucose oxidation is of central importance for practical applications such as glucose fuel cell. Pt-decorated nanoporous gold (NPG-Pt), created by depositing a thin layer of Pt on NPG surface, was proposed as an active electrode for glucose electrooxidation in neutral and alkaline solutions. The structure and surface properties of NPG-Pt were characterized by scanning electron microscopy (SEM), transmission electron microscopy (TEM), X-ray powder diffraction (XRD), and cyclic voltammetry (CV). The electrocatalytic activity toward glucose oxidation in neutral and alkaline solutions was evaluated, which was found to depend strongly on the surface structure of NPG-Pt. A direct glucose fuel cell (DGFC) was performed based on the novel membrane electrode materials. With a low precious metal load of less than 0.3 mg cm-2 Au and 60 µg cm-2 Pt in anode and commercial Pt/C in cathode, the performance of DGFC in alkaline is much better than that in neutral condition.

[Ecological characteristics of Artemisia halodendron community and population on Horqin sandy land].

Based on the analysis of species important values and Shannon-Wiener index of Artemisia halodendron community on different type sandy lands in Horqin, A. halodendron community was classified into three types, i. e., A. halodendron - annual herbage, A. halodendron - perennial grass, and A. frigida - A. scoparia + perennial grass, which distributed on shifting sandy land, semi-fixed sandy land, and fixed sandy land, respectively. With the sand fixed, the community succession was ranked from A. halodendron - annual herbage (pioneer stage, coverage < 10%, Shannon-Wiener index 0. 33) to A. halodendron - perennial grass (coverage 30% to approximately 35%, Shannon-Wiener index 0. 56), and then to A. frigida - A. scoparia + perennial grass (steppe community, coverage 40% to approximately 45%, Shannon-Wiener index 0. 59). The A. halodendron population on shifting sandy land and that planted 5 years ago showed growing age distribution, that planted 18 years ago showed stable age distribution, and that on semi-fixed and fixed sandy lands showed declining age distribution. The results proved that A. halodendron populations had different ecological effects on A. halodendron community.