Bio-Inspired Superhydrophilic Self-Assembled Coronavirus-Like Pt-WC/CNT for Hydrogen Evolution Reaction.

This study presents a novel approach to enhance the catalytic activity of composite materials by promoting active surface exposure and improving hydrogen transfer performance. Through a self-assembly route involving tailored gas-solid and galvanic replacement reactions, Pt-WC/CNT catalysts with superhydrophilicity and coronavirus-like structure are synthesized. These unique structural features contribute to a remarkable enhancement in the electrocatalytic performance of the hydrogen evolution reaction (HER). Notably, the Pt-WC/CNT catalyst exhibits an outstanding intrinsic activity and efficient bubble transfer properties, leading to a high turnover frequency of 34.97 H2 ·s-1 at an overpotential of 100 mV. This value is 4.8 times higher than that achieved by commercial Pt/C catalysts (7.30 H2 ·s-1 ), establishing Pt-WC/CNT as one of the most active catalysts reported to date. Moreover, the combination of gas-solid and galvanic replacement reactions in the synthesis process offers a scalable route for the production of Pt-loading controllable composite catalysts, thus challenging the dominance of commercial Pt/C catalysts.

Efficient Regulation of the Cross-Linking Structure in Polyurethane: Achieving Outstanding Processing and Mechanical Properties for a Wind Turbine Blade.

Although epoxy resin has been extensively used in the field of wind turbine blades, polyurethane has attracted much attention in recent years, due to its potential value of better fatigue resistance, lower processing viscosity and higher strength than epoxy resin blades. Herein, we construct a dense cross-linking structure in polyurethane (PU) based on different amounts of hydroxypropyl methacrylate (HPMA) with low processing viscosity and excellent mechanical properties. By increasing the content of HPMA, the thermal stability of PU is enhanced, but the micro-morphology does not change significantly. When the content of HPMA is 50 g (in 200 g copolymer), the PU sample PH-50 exhibits a viscosity of 70 MPa·s and a gelation time of 120 min at 25 °C, which is sufficient to complete processes like pouring and filling. By post-curing the PH-50 at 80 °C for 2 h, the heat distortion temperature can reach 72 °C, indicating the increase of temperature resistance. The PU copolymers also have excellent mechanical and dynamic thermo-mechanical properties due to the cross-linking structure between PU chains and poly-HPMA chains. Additionally, the PU copolymer has excellent compatibility with various glass fiber fabrics (GFF), showing a good match in the vacuum infusion experiment and great properties in the mechanical test. By compounding PH-50 with GFF, the composite with high strength is easily prepared for a wind turbine blade in various positions. The tensile strengths of the composites are all over 1000 MPa in the 0° direction. Such composites are promising for the future development of wind turbine blades that meet the stringent requirements for outstanding processing and mechanical properties.

Modulating Dominant Facets of Pt through Multistep Selective Anchored on WC for Enhanced Hydrogen Evolution Catalysis.

Facilitating the exposure of the active crystal facets on the surfaces of composite catalysts is a representative route to promote catalytic activity. Based on a tailored galvanic replacement reaction, herein, a self-assembly route is reported to prepare Pt-WC/CNT with Pt (200) preferential orientation and well-dispersed structure, which are capable of substantially boosting electrocatalysis in hydrogen evolution reaction (HER). Formation mechanism reveals that the (200)-dominated Pt-based catalysts form in galvanic replacement reaction through selective anchored on WC, and the multistep galvanic replacement process plays a critical role to realize the Pt (200)-dominated growth in higher Pt loading catalyst. These unique structural features endow the Pt-WC/CNT with a high turnover frequency of 94.18 H2·s-1 at 100 mV overpotential, 7-fold higher than that of commercial Pt/C (13.55 H2·s-1), ranking it among the most active catalysts. In addition, this method, which combines with gas-solid reaction and galvanic replacement reaction, paves the way to scalable synthesis as Pt facets-controllable composite catalysts to challenge commercial Pt/C.

Fabrication of MgAl LDH@graphene oxide nanohybrids and their effect on the thermal stability and crystallization behavior of polypropylene.

The co-precipitation method is used to fabricate layered double hydroxide (LDH) nanohybrids with surface engineering of graphene oxide (GO) by radially grafting borate-LDH (BLDH) to BLDH@GO nanosheets, aiming at improving the surface characteristics and compatibility of LDH with the polymer matrix. The results prove the successful fabrication of BLDH@GO and LDH@GO nanosheets. The nanosheets are mixed into polypropylene (PP) by melt blending to study the structure and properties of the composites. The PP composites with BLDH@GO and BLDH have both exfoliation structures and aggregation structures, and the two nanosheets show enhanced interfacial interactions with the PP matrix compared with LDH and LDH@GO. The initial decomposition temperatures of the PP composites are lower than those of the neat PP, but the thermal degradation temperatures of the PP composites are higher. Compared with the other samples, BLDH@GO provides a higher nucleation density, reflected in a smaller spherulite size and a higher crystallization temperature confirmed by the differential scanning calorimetry (DSC) results. BLDH@GO shifts the crystallization temperature of PP to higher values (compared to the neat PP) due to the nucleation effect, which is in line with the increase in the nucleation density detected by polarized optical microscopy (POM).

Occurrence and fate of antibiotics and heavy metals in sewage treatment plants and risk assessment of reclaimed water in Chengdu, China.

Aim of this study was to provide an up-to-date assessment of the heavy metals and antibiotics in reclaimed water in Chengdu, China. 3 sewage treatment plants (STPs) and 1 constructed wetland (CW) were first taken as the research objects. The total concentration and reduction change rule of heavy metals and antibiotics in the process of reclaimed water production were investigated. The possible health risks to ecological environment and human body were evaluated. For the treatment process, the Cyclic Activated Sludge System (CASS) used in A sewage treatment plant (STP A) had the best removal effect for heavy metals. When the proportion of industrial wastewater in the influent was relatively high, the heavy metal pollution level was alert. Ofloxacin (OFX) and roxithromycin (ROX) were the most abundant antibiotics in reclaimed water. After being removed by the sewage treatment system, OFX concentrations changed, but several of them remained in reclaimed water. Negative removal of ROX occurred. This is because macrolides were wrapped in human feces, whose concentration increased as feces disperse and hydrolyze. Compared with CASS (20.02%) and Anaerobic-Anoxic-Oxic process (A2/O 34.16%), the average removal rate of antibiotics from the A2/O accompanied by Membrane Bio-Reactor (71.1%) and CW (54.95%) was higher. When the proportion of domestic sewage in wastewater was high, antibiotics in reclaimed water had higher ecological risk. OFX had the highest ecological risk for non-target aquatic organisms. It was assessed that the heavy metals and antibiotics studied did not pose a carcinogenic or non-carcinogenic risk to human health.

Synthesis, characterization, and crystallization behaviors of poly(D-lactic acid)-based triblock copolymer.

Poly(D-lactic acid) (PDLA) with different polyethylene glycol (PEG) segment synthesized PDLA-PEG-PDLA triblock copolymer through the ring-opening reaction of D-LA and PEG will be used as a toughening modifier. The microstructure, crystal structures and crystallization behaviors of this triblock copolymer were investigated by Fourier transform infrared (FTIR) spectroscopy, nuclear magnetic resonance (NMR) spectroscopy, X-ray diffraction (XRD), differential scanning calorimetry (DSC) and polarized optical microscopy (POM). The triblock copolymer is synthesized from the appearance of CH2 stretching vibration peak at 2910 cm-1 and C-O stretching vibration peak at 1200 cm-1 from PEG in FTIR spectra. Moreover, the chemical shift that is about 3.6 ppm in 1H NMR and 68.8ppm in 13C NMR proves this matter. The results of XRD and DSC reveal that PDLA and PEG are crystallized separately, and are not fully compatible, and microphase separation has occurred in this triblock copolymer. PEG can induce the triblock copolymer to accelerate the rate of crystallization, allowing it to crystallize more completely in the same amount of time. When the molecular weight of PEG is 6000 or the ratio of D-LA/PEG is 1/1, the crystallizability of PDLA-PEG-PDLA triblock copolymer is the best.

The effect of thermo-oxidative ageing on crystallization, dynamic and static mechanical properties of long glass fibre-reinforced polyamide 10T composites.

The performances and microstructure of long glass fibre-reinforced polyamide 10T (PA10T/LGF) composites that experienced different ageing temperatures (160 and 200°C) with increasing ageing time are characterized by differential scanning calorimetry (DSC), mechanical analysis, thermogravimetric analysis (TGA) and scanning electron microscopy to probe the correlation between properties of the composites and thermo-oxidative ageing. The DSC results show that PA10T/LGF composites occur on degradation, the fracture of molecular chains and the destruction of crystallization structure, which leads to the crystallization and melting peaks of PA10T/LGF composites to shift to high temperature. On the basis of dynamic mechanical analysis data, the reduction of the interfacial bonding between the glass fibre and PA10T matrix and the motion of molecular chain segments result in the thermo-oxidative ageing of composites. According to the calculation of activation energy (E), thermo-oxidative temperature and ageing time can bring about the decline of the E value, proving the deterioration in performance of PA10T/LGF composites. In view of TGA, the increase in the thermo-oxidative temperature and ageing time promotes the degradation of PA10T/LGF composites. The tensile, flexural and notched impact strengths of PA10T/LGF composites decline with prolonging the ageing temperature and time. The surface of materials produces some microcracks and the cross-section surface of PA10T/LGF composites becomes rougher.

Novel Intumescent Flame Retardant Masterbatch Prepared through Different Processes and Its Application in EPDM/PP Thermoplastic Elastomer: Thermal Stability, Flame Retardancy, and Mechanical Properties.

In this work, the ethylene-propylene-diene monomer/polypropylene (EPDM/PP) thermoplastic elastomer filled with intumescent flame retardants (IFR) is fabricated by melting blend. The IFR are constituted with melamine phosphate-pentaerythritol (MP/PER) by compounding and reactive extruding, respectively. The effects of two kinds of MP/PER with different contents on the thermal stability, flame retardancy, and mechanical properties of materials are investigated by Fourier transform infrared (FTIR) spectroscopy, thermogravimetric analysis (TGA), limiting oxygen index (LOI), UL-94, cone calorimeter test (CCT), and scanning electron microscopy (SEM). FTIR results show that the reactive extruded MP/PER partly generates melamine pyrophosphate (MPP) compared with compound masterbatches. TGA data indicate that the best thermal stability is achieved when the molar ratio of MP/PER reaches 1.8. All the reactive samples show a higher flame retardancy than compound ones. The CCT results also exhibit the same trend as above in heat release and smoke production rate. The EPDM/PP composites filled with 30 and 35% reactive MP/PER exhibit the improved flame retardancy but become stiffer and more brittle. SEM photos display that better dispersion and smaller particle size are obtained for reactive samples.