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The phase structure and evolution of polypropylene (PP)/poly(ethylene-1- octene) copolymer (PEOc) blends during heat preservation process under quiescent condition were studied using scanning electron microscopy (SEM). The structure parameters, such as the average area diameter d, characteristic length L, and average characteristic length L, of the dispersed phase in PP/ PEOc blends were calculated by pattern analysis of SEM images. Moreover, the potential fractal behavior of the phase structure and morphology of polymer blends during the process was discussed. The histograms of P( L( t)/ L) obtained at various time fell on a master curve, demonstrating the self-similar growth of the phase structure of the blends during heat preservation process. [ABSTRACT FROM AUTHOR]

Binary blends based on polypropylene and poly(ethylene- co-octene) were prepared in a co-rotating twin-screw extruder. A stretching process was carried out afterwards in the melt state at the extruder's exit to study the effect of stretching on morphological structures and mechanical properties. The morphological structures of the blends were investigated by scanning electron microscopy and small-angle X-ray scattering. The structure parameters, the correlation distance, the average chord lengths, and the Porod's index, obtained by the Debye-Bueche statistical theory of scattering were used to characterize the morphological structures. In addition, the relationship of mechanical properties with the structure parameters was also studied and some results were acquired. [ABSTRACT FROM AUTHOR]

Highlights: Design and fabrication of MXene-based soft actuators with angle-independent structural color. The nanostructured MXene can not only facilitate the formation of short-range ordered 3D amorphous photonic crystals, but also help significantly improve structural color saturation. The soft actuators exhibit brilliant angle-independent structural color, ultrafast actuation and recovery speeds in response to vapor. In nature, many living organisms exhibiting unique structural coloration and soft-bodied actuation have inspired scientists to develop advanced structural colored soft actuators toward biomimetic soft robots. However, it is challenging to simultaneously biomimic the angle-independent structural color and shape-morphing capabilities found in the plum-throated cotinga flying bird. Herein, we report biomimetic MXene-based soft actuators with angle-independent structural color that are fabricated through controlled self-assembly of colloidal SiO2 nanoparticles onto highly aligned MXene films followed by vacuum-assisted infiltration of polyvinylidene fluoride into the interstices. The resulting soft actuators are found to exhibit brilliant, angle-independent structural color, as well as ultrafast actuation and recovery speeds (a maximum curvature of 0.52 mm−1 can be achieved within 1.16 s, and a recovery time of ~ 0.24 s) in response to acetone vapor. As proof-of-concept illustrations, structural colored soft actuators are applied to demonstrate a blue gripper-like bird's claw that can capture the target, artificial green tendrils that can twine around tree branches, and an artificial multicolored butterfly that can flutter its wings upon cyclic exposure to acetone vapor. The strategy is expected to offer new insights into the development of biomimetic multifunctional soft actuators for somatosensory soft robotics and next-generation intelligent machines. [ABSTRACT FROM AUTHOR]

Developing hydrogel actuators with excellent driving performance and extended lifespan remains challenging. Ti3C2Tx MXene, as a two-dimensional nanomaterial with a unique layered structure, has attracted widespread attention in flexible hydrogel actuators for its excellent optical absorption properties and tunable surface functionality. However, MXene faces difficulties in dispersion and is prone to oxidation, which significantly hinders the development and use of MXene-based hydrogel actuators. In this study, we fabricated a near-infrared light-driven hydrogel actuator with rapid photo responsiveness and antioxidative properties by incorporating modified MXene with antioxidant characteristics and the pore-forming agent polyvinyl alcohol into the poly(N-isopropylacrylamide) (PNIPAM) hydrogel system. We functionalized MXene nanosheets with (3-aminopropyl)triethoxysilane (APTES), effectively enhancing antioxidative properties, preventing structural degradation caused by spontaneous oxidation, and improving surface properties. This enhanced the dispersion stability of MXene in the system and extended its lifespan from 7 days to over two weeks. The hydrophilic polyvinyl alcohol chains served as drainage channels during hydrogel contraction, imparting the hydrogel with rapid driving capabilities (127.1° s−1). Additionally, leveraging the fast response characteristics, we designed an octopus-inspired light-driven soft swimmer and gripper. This work provides novel insights into the application of intelligent responsive hydrogels in biomimetic and practical scenarios.Graphical abstract: Developing hydrogel actuators with excellent driving performance and extended lifespan remains challenging. Ti3C2Tx MXene, as a two-dimensional nanomaterial with a unique layered structure, has attracted widespread attention in flexible hydrogel actuators for its excellent optical absorption properties and tunable surface functionality. However, MXene faces difficulties in dispersion and is prone to oxidation, which significantly hinders the development and use of MXene-based hydrogel actuators. In this study, we fabricated a near-infrared light-driven hydrogel actuator with rapid photo responsiveness and antioxidative properties by incorporating modified MXene with antioxidant characteristics and the pore-forming agent polyvinyl alcohol into the poly(N-isopropylacrylamide) (PNIPAM) hydrogel system. We functionalized MXene nanosheets with (3-aminopropyl)triethoxysilane (APTES), effectively enhancing antioxidative properties, preventing structural degradation caused by spontaneous oxidation, and improving surface properties. This enhanced the dispersion stability of MXene in the system and extended its lifespan from 7 days to over two weeks. The hydrophilic polyvinyl alcohol chains served as drainage channels during hydrogel contraction, imparting the hydrogel with rapid driving capabilities (127.1° s−1). Additionally, leveraging the fast response characteristics, we designed an octopus-inspired light-driven soft swimmer and gripper. This work provides novel insights into the application of intelligent responsive hydrogels in biomimetic and practical scenarios. [ABSTRACT FROM AUTHOR]

Three-dimensional (3D) molecularly imprinted polymer (MIP) arrays were used for electrochemical sensor to detect sulfadimidine (SM2) residue in food. NiCo2O4 nanoneedle arrays were decorated on the free-standing and highly conductive 3D graphene by a hydrothermal process. Polypyrrole (PPy) was coated onto NiCo2O4 nanoneedle arrays via electropolymerization in the presence of template molecule SM2 to obtain MIP/NiCo2O4 nanoneedle/3D graphene electrode. The desirable detectability of the composite electrode can be ascribed to the unique structure and the synergistic effects of the components: Nanoneedle arrays on 3D graphene offered the matrix to MIP and each nanoneedle as sensing unit was accessible to analyte, resulting in high specific surface area, desirable conductivity, short ion diffusion path and excellent adsorption capacity, which could powerfully boost the electrochemical property for the detection of SM2. Under optimized conditions, a wide linear range over SM2 of 0.2-1000 ng/mL with a detection limit of 0.169 ng/mL (S/N = 3) was obtained. The developed sensor also had favorable recovery of 92.3-102.23% and the relative standard deviation of 2.27-4.10%. The MIP array sensor provided an efficient tool for the selective and rapid detection of SM2 in food. [ABSTRACT FROM AUTHOR]

PPy/PANI double-layer nanotubes anchored reduced graphene oxide (rGO) nanosheets with three-dimensional architecture (3DGP) have been obtained for supercapacitors applications. The freestanding electrode yields specific capacitance (542 F g at current density of 1 A/g) and excellent cycle stability (92.1% capacitance retention after 2000 cycles in a three-electrode cell configuration). The further assembled symmetric supercapacitor device exhibits a high energy density of 20.8 W h kg at a power density of 250 W kg and good cycle stability (capacitance loss of 7% up to 2000 cycles). The exceptional electrochemical performance of 3DGP can be ascribed to the unique structure and the synergistic effects of the components: (1) Integrating the highly capacitance matrix PPy/PANI coaxial nanotubes hybrid in rGO to enhance the reversible faradic reactions can boost the utilization rate of the electrode materials and circumventing the predicament of pseudo materials. (2) The desirable π- π interactions between highly conductive rGO films and polymer chains construct a high-performance network, which facilitates rapid transport of the electrolyte ions in the electrode. (3) The as-prepared electrode materials fabricated into electrodes directly decrease the 'dead weight,' for the addition of binder and conductive agents can be avoided. [ABSTRACT FROM AUTHOR]

Here, a supramolecular self-assembly hydrogel was designed for SnO-based anode through electrostatic interaction and ionic bonding between poly(allylamine hydrochloride) (PAH) chain and gelator phytic acid. Microrheology measurement was employed to investigate the self-sorting mechanism of the hierarchical nanostructured PAH. Results confirmed that ionically cross-link PAH improves the structural integrity of SnO nanospheres due to the reversible ionic bonding and thus increases the lifetime of the electrodes obviously. Besides, multi-walled carbon nanotubes (MWCNTs) were applied to improve the electrochemical performance of hollow SnO nanospheres due to their high conductivity. Results confirmed that the conductive network constructed by MWCNTs reduces the polarization of the composites while increases the specific capacity of the electrodes. Attributed to the synergistic effect of PAH-60 and MWCNTs, the composite electrodes show excellent electrochemical performance with a reversible capacity of 574 mAh g after 100 cycles at 100 mA g, a discharge capacity of 321 mAh g at 2000 mA g and a spring-back capacity of 506 mAh g at 200 mA g. Additionally, the prepared composite electrodes were observed to have a complete network structure after rate capability test, demonstrating a superior structural stability. [ABSTRACT FROM AUTHOR]

In this work, we reported the highly ordered NiCoO nanoneedle@polypyrrole arrays anchored on three-dimensional graphene (NiCoO@PPy/3D graphene) for high-sensitivity detection of trace lead ions (Pb). The 3D graphene was prepared by a hydrothermal process and then decorated with NiCoO nanoneedle arrays by another hydrothermal process. This two-step hydrothermal method is simple and mild. Furthermore, the highly conductive PPy was coated on NiCoO via a chemical vapor-phase polymerization to prepare NiCoO@PPy/3D graphene. The free-standing NiCoO@PPy/3D graphene can be directly utilized as 3D electrochemical working electrode without being decorated onto working electrode like Au and glassy carbon electrode. High conductivity, large specific surface area, short ion diffusion path and excellent adsorption capacity of NiCoO@PPy/3D graphene efficiently improved electrochemical property for the detection of Pb. Using square-wave anodic stripping voltammetry (SWASV), a linear range between the currents and the concentrations of Pb of 0.0125-0.709 μM with a high sensitivity of 115.621 μA μM was obtained. The limit of detection can reach to 0.2 nM. In addition, the fabricated sensor of Pb also had good selectivity, reproducibility and long-term stability. Finally, NiCoO@PPy/3D graphene electrode was utilized for determining Pb in tap water sample using the standard addition method, revealing a promising application for the quantitative detection of certain concentration ranges of Pb in real sample. [ABSTRACT FROM AUTHOR]

In order to discuss the effect of polymer coating layer on the Sn anode, the composition and morphology of the solid electrolyte interphase (SEI) film on the surface of Sn and Sn@PEO anode materials have been investigated. Compared with the bare cycled Sn electrode, the SEI on the surface of cycled Sn@PEO electrode is thinner, smoother, and more stable. Therefore, the Sn@PEO nanoparticles can basically keep the original appearance during cycling. Based on the results obtained from X-ray photoelectron spectroscopy (XPS), the SEI formed on the Sn@PEO electrode is characterized by inorganic components (LiCO)-rich outer layer and organic components-rich inner which could make the SEI more stable and inhibit the electrolyte immerging into the active materials. In particular, the elastic ion-conductive polyethylene oxide (PEO) coating could increase the toughness of SEI and allow the SEI to endure the stress variation in repetitive lithium insertion and extraction process. As a result, the Sn@PEO electrodes show significantly better capacity retention than bare Sn electrodes. The findings can serve as the theoretical foundation for the design of lithium-ion battery electrode with high energy density and long cycle life. [ABSTRACT FROM AUTHOR]

A novel MWCNT/long nanotubular TiO(B) loaded with SnO nanocrystals (SnONC/TiO(B)NT/MWCNT) ternary composite has been prepared by two-step hydrothermal method and used as the anode material for the first time. In this work, the mechanical stirring improved the diffusion and surface reaction rates of reactants and promoted the appearance of longer intermediate TiO(B) nanosheets, leading to the formation of TiO(B) nanotubes with a length of ~9 μm. Among the SnONC/TiO(B)NT/MWCNT composite, the wrapping and mechanical supporting functions of TiO(B) nanotubes can effectively avoid the pulverization and aggregation of SnO nanocrystals (SnONC) in lithium-ion charging and discharging process. Moreover, the synergistic effects of nanotubular TiO(B) coating layer and three-dimensional interconnected network structure composed of TiO(B) nanotubes and MWCNT were taken to mitigate volume expansion of SnONC and improve the transport of lithium ion and electron in the network. Tested as anode materials, the SnONC/TiO(B)NT/MWCNT composite maintained 211 mAh g at 3000 mA g after three testing processes with alternative current density of 200 and 3000 mA g and could rebound to 338 mAh g at a current density of 200 mA g, indicating an effective way to optimize electrochemical properties of SnO as anode material. [ABSTRACT FROM AUTHOR]

Anaerobic oxidation of methane (AOM) coupled to nitrite reduction (AOM-NIR) is ecologically significant for mitigating the methane-induced greenhouse effect. The microbes responsible for this reaction, NC10 bacteria, have been widely detected in diverse ecosystems. However, some defects were discovered in the commonly used NC10-specific primers, 202F and qP1F. In the present work, the primers were redesigned and improved to overcome the defects found in the previous primers. A new nested PCR method was developed using the improved primers to amplify 16S ribosomal RNA (rRNA) genes from NC10 bacteria. In the new nested PCR method, the qP1mF/1492R and 1051F/qP2R primer sets were used in the first and second rounds, respectively. The PCR products were sequenced, and more operational taxonomic units (OTUs) of the NC10 phylum were obtained using the new primers compared to the previous primers. The sensitivity of the new nested PCR was tested by the serial dilution method, and the limit of detection was approximately 10 copies g dry sed. for the environmental samples compared to approximately 10 copies g dry sed. by the previous method. Finally, the improved primer, qP1mF, was used in quantitative PCR (qPCR) to determine the abundance of NC10 bacteria, and the results agreed well with the activity of AOM-NIR measured by isotope tracer experiments. The improved primers are able to amplify NC10 16S rRNA genes more efficiently than the previous primers and useful to explore the microbial community of the NC10 phylum in different systems. [ABSTRACT FROM AUTHOR]

Conducting polymer hydrogels are emerging as a promising class of materials that combine the advantageous features of conventional hydrogels and organic conductors, and would potentially be used in many applications, especially for energy storage devices. To overcome the drawbacks of conventional synthesis, this work describes the use of amino trimethylene phosphonic acid as the gelator and dopant for rapidly fabricating hierarchical nanostructured polyaniline (PAni) hydrogel with excellent electronic conductivity and electrochemical properties. Owing to 3D porous nanostructures and high surface area, the PAni hydrogel exhibits potential as high-performance supercapacitor electrodes with specific capacitance over 420 F g. Furthermore, the rapidly formed PAni hydrogel was first used for 3D multilayer printing of micro-patterns due to the unique synthesis method and desirable processability. Taken together, these results suggest that the PAni hydrogel networks exhibit highly useful for a broad range of applications. [ABSTRACT FROM AUTHOR]

Nitrite-dependent anaerobic methane oxidation (n-damo) is a newly discovered bioprocess that reduces nitrite to dinitrogen with methane as electron donor, which has promising potential to remove nitrogen from wastewater. In this work, a lab-scale sequencing batch reactor (SBR) was operated for 609 days with methane as the sole external electron donor. In the SBR, nitrite in synthetic wastewater was removed continuously; the final volumetric nitrogen removal rate was 12.22±0.02 mg N L day and the percentage of nitrogen removal was 98.5 ± 0.2 %. Microbial community analysis indicated that denitrifying methanotrophs dominated (60-70 %) the population of the final sludge. Notably, activity testing and microbial analysis both suggested that heterotrophic denitrifiers existed in the reactor throughout the operation period. After 609 days, the activity testing indicated the nitrogen removal percentage of heterotrophic denitrification was 17 ± 2 % and that of n-damo was 83 ± 2 %. A possible mutualism may be developed between the dominated denitrifying methanotrophs and the associated heterotrophs through cross-feed. Heterotrophs may live on the microbial products excreted by denitrifying methanotrophs and provide growth factors that are required by denitrifying methanotrophs. [ABSTRACT FROM AUTHOR]

In order to optimize the electrode system of lithium-ion batteries (LIBs) for problems like lithium-ion diffusion, electron transport, and large volume change during cycling processes, a novel three-dimensional (3D) hybrid FeO nanotube array anode coated by polypyrrole (FeO@PPy) is synthesized via a sacrificial template-accelerated hydrolysis method followed by a chemical vapor-phase polymerization process. In the hollow core-shell nanostructures, the conducting PPy layer could not only facilitate the electron transport, but also force the core to expand inward into the hollow space, which allows for free volume expansion of the FeO without mechanical breaking. Besides, the static outer surface is contributed to form a stable solid electrolyte interface film. As a result, the integration of 3D hybrid nanostructure electrode is capable of retaining a high capacity of 665 mA h g after 150 cycles with a coulombic efficiency of above 97 %, revealing better cycling properties compared with bare FeO nanotube arrays' anode. This nanoengineering strategy is proven to be an ideal candidate for the development of high-performance anode for LIBs. [ABSTRACT FROM AUTHOR]

Microbial-driven biogeochemical cycles in wetlands impacted by global warming pose a potential downstream eutrophication risk. However, the consequences of ongoing warming on the functional and metabolic potential of sediment microbial communities are largely unknown. We incubated sediment samples under both ambient temperature conditions (control) and simulated warming conditions of 5°C above ambient temperature (warmed) using a novel field microcosm system. In warmed samples, we observed in situ a decreased thickness of the oxidized sediment layer and associated lower sediment redox potential. GeoChip 4.0, a comprehensive functional gene microarray, demonstrated that many functional genes that are involved in oxidation-reduction reactions and in phosphorus (P) degradation were preferentially enriched under warming conditions. The enriched genes included those genes encoding carbon monoxide dehydrogenase, acetyl-CoA carboxylase biotin carboxylase ( ppc), and ribulose-1,5-bisphosphate carboxylase (Rubisco) for carbon fixation; nitrate reductases ( narG) and nitrous oxide reductases ( nosZ) for denitrification; cytochrome c for metal reduction; and exopolyphosphatase ( ppx) for polyphosphate degradation. The redox potential was one of the most significant parameters linked to microbial functional gene structure. These results demonstrate that the enhanced hypoxia and anaerobic metabolic pathways accelerated sediment P mobilization in freshwater wetland subject to warming, raising the potential of water eutrophication. [ABSTRACT FROM AUTHOR]

Nitrite-dependent anaerobic methane oxidation (n-damo) is a newly discovered biological process that couples anaerobic oxidation of methane (AOM) to nitrite reduction. In this study, three different inocula, methanogenic sludge, paddy soil, and freshwater sediment were used to enrich n-damo bacteria in three sequencing batch reactors (SBRs), and three n-damo enrichment cultures, C1, C2 and C3, were obtained, respectively. After 500 days of incubation, Methylomirabilis oxyfera-like bacteria and n-damo activities were observed in cultures C1, C2, and C3, and the specific activities were 0.8 ± 0.1, 1.4 ± 0.1, and 1.0 ± 0.1 μmol CH h g VSS, respectively. The copy numbers of 16S rRNA genes from cultures C1, C2, and C3 were 5.0 ± 0.4 × 10, 6.1 ± 0.1 × 10, and 1.0 ± 0.2 × 10 copies g dry weight, respectively. The results indicated that paddy soil is an excellent inoculum for n-damo bacterial enrichment. This work expanded the alternative source of n-damo inoculum and benefited the further research of n-damo process. [ABSTRACT FROM AUTHOR]

Nitrite-dependent anaerobic methane oxidation (n-damo) is mediated by bacteria that anaerobically oxidize methane coupled with nitrite reduction and is a potential bioprocess for wastewater treatment. In this work, the effect of reactor configuration on n-damo bacterial cultivation was investigated. A magnetically stirred gas lift reactor (MSGLR), a sequencing batch reactor (SBR), and a continuously stirred tank reactor (CSTR) were selected to cultivate the bacteria. Microbial community was monitored by using quantitative PCR, 16S rRNA gene sequencing, pmoA gene sequencing, and fluorescence in situ hybridization (FISH). The effects of substrate inhibition, methane mass transfer, and biomass washout in the three reactors were focused on. The results indicated that the MSGLR had the best performance among the three reactor systems, with the highest total and specific n-damo activities. Its maximum volumetric nitrogen removal rate was up to 76.9 mg N L day, which was higher than previously reported values (5.1-37.8 mg N L d). [ABSTRACT FROM AUTHOR]

Nanostructured hollow Sn-Cu multi-phase composite nanoparticles anode that contains Sn and CuSn was synthesized via galvanic replacement reaction using Sn nanoparticles as a sacrificial template. The sacrificial oxidation of Sn and simultaneous reduction of Cu on the surface because of the redox potential difference is proposed to account for the formation of hollow Sn-Cu nanostructures. The structural evolution of the Sn-Cu hollow nanoparticle, in the process of galvanic replacement and structure, composition changes during charge/discharge processes were studied based on scanning electron microscope, X-ray powder diffraction, transmission electron microscopy, and energy dispersive X-ray spectroscopy investigations. The electrochemical properties of the samples were evaluated by galvanostatic discharge-charge cycling, cyclic voltammetry, and electrochemical impedance spectroscopy. Compared with solid Sn-Cu nanoparticles, hollow Sn-Cu nanoparticles showed better capacity retention. The improved electrochemical performance may be attributed to the stable hollow structure and the combination of CuSn. The facile solution-based process and excellent cycling stability show great potential of the multi-phase Sn-Cu hollow composite nanoparticles as an anode material for lithium-ion batteries. [ABSTRACT FROM AUTHOR]

The influence of quiescent molten-state annealing process on the phase structure and morphology of poly(propylene)/poly(ethylene-co-octene) blends with co-continuous morphology was studied using scanning electron microscopy (SEM). The structure parameter called characteristic length ( L) was calculated by the pattern analysis of SEM micrographs to describe morphological variation with annealing time during molten-state annealing process under quiescent condition. Moreover, the potential fractal behavior of the phase structure and morphology of PP/PEOc = 50/50 blend during the process were discussed. The histograms of P( L/ L) obtained at various annealing time fell on a master curve, demonstrating the self-similar growth of the phase structure of the blends during quiescent molten-state annealing process. [ABSTRACT FROM AUTHOR]

This work was aimed at studying the phase structure and evolution of polypropylene (PP)/poly(ethylene-1-octene) copolymer (PEOc) blends with droplet/matrix morphology using scanning electron microscopy (SEM) during quiescent molten-state annealing process. The structure parameters, such as the area diameter, d, and number average diameters, D, of the dispersed phase in PP/PEOc blends were calculated by pattern analysis of SEM images. Moreover, the potential fractal behavior of the phase structure and morphology of PP/PEOc = 80/20 blend during the process was discussed. The histograms of $$ P\left( {{d_p \left/ {{{{\overline{d}}_p}}} \right.}} \right) $$ obtained at various annealing time fell on a master curve, demonstrating the self-similar growth of the phase structure of the blends during quiescent molten-state annealing process. [ABSTRACT FROM AUTHOR]

A letter to the editor is presented in response to the article "The Thermodynamic Behavior and Morphology of PP/POE Blends Prepared by Melt- and Solution-mixing Methods," by Jing Zhao, Xingming Shuai, Li Wang, Xinqiang Tang, Xinhua Xu, Jing Sheng, and Dinghai Huang published online March 11, 2009.

Uniform dispersion of two-dimensional (2D) graphene materials in polymer matrices remains challenging. In this work, a novel layer-by-layer assembly strategy was developed to prepare a sophisticated nanostructure with highly dispersed 2D graphene oxide in a three-dimensional matrix consisting of one-dimensional bacterial cellulose (BC) nanofibers. This method is a breakthrough, with respect to the conventional static culture method for BC that involves multiple in situ layer-by-layer assembly steps at the interface between previously grown BC and the culture medium. In the as-prepared BC/GO nanocomposites, the GO nanosheets are mechanically bundled and chemically bonded with BC nanofibers via hydrogen bonding, forming an intriguing nanostructure. The sophisticated nanostructure of the BC/GO leads to greatly enhanced mechanical properties compared to those of bare BC. This strategy is versatile, facile, scalable, and can be promising for the development of high-performance BC-based nanocomposite hydrogels. [ABSTRACT FROM AUTHOR]