Zoonotic pathogens identified in rodents and shrews from four provinces, China, 2015-2022.

Rodents and shrews are major reservoirs of various pathogens that are related to zoonotic infectious diseases. The purpose of this study was to investigate co-infections of zoonotic pathogens in rodents and shrews trapped in four provinces of China. We sampled different rodent and shrew communities within and around human settlements in four provinces of China and characterised several important zoonotic viral, bacterial, and parasitic pathogens by PCR methods and phylogenetic analysis. A total of 864 rodents and shrews belonging to 24 and 13 species from RODENTIA and EULIPOTYPHLA orders were captured, respectively. For viral pathogens, two species of hantavirus (Hantaan orthohantavirus and Caobang orthohantavirus) were identified in 3.47% of rodents and shrews. The overall prevalence of Bartonella spp., Anaplasmataceae, Babesia spp., Leptospira spp., Spotted fever group Rickettsiae, Borrelia spp., and Coxiella burnetii were 31.25%, 8.91%, 4.17%, 3.94%, 3.59%, 3.47%, and 0.58%, respectively. Furthermore, the highest co-infection status of three pathogens was observed among Bartonella spp., Leptospira spp., and Anaplasmataceae with a co-infection rate of 0.46%. Our results suggested that species distribution and co-infections of zoonotic pathogens were prevalent in rodents and shrews, highlighting the necessity of active surveillance for zoonotic pathogens in wild mammals in wider regions.

Effects of Styrene-Acrylic Sizing on the Mechanical Properties of Carbon Fiber Thermoplastic Towpregs and Their Composites.

Thermoplastic towpregs are convenient and scalable raw materials for the fabrication of continuous fiber-reinforced thermoplastic matrix composites. In this paper, the potential to employ epoxy and styrene-acrylic sizing agents was evaluated for the making of carbon fiber thermoplastic towpregs via a powder-coating method. The protective effects and thermal stability of these sizing agents were investigated by single fiber tensile test and differential scanning calorimetry (DSC) measurement. The results indicate that the epoxy sizing agent provides better protection to carbon fibers, but it cannot be used for thermoplastic towpreg processing due to its poor chemical stability at high temperature. The bending rigidity of the tows and towpregs with two styrene-acrylic sizing agents was measured by cantilever and Kawabata methods. The styrene-acrylic sized towpregs show low torque values, and are suitable for further processing, such as weaving, preforming, and winding. Finally, composite panels were fabricated directly from the towpregs by hot compression molding. Both of the composite panels show superior flexural strength (>400 MPa), flexural modulus (>63 GPa), and interlaminar shear strength (>27 MPa), indicating the applicability of these two styrene-acrylic sizing agents for carbon fiber thermoplastic towpregs.

Complexes of polydopamine-modified clay and ferric ions as the framework for pollutant-absorbing supramolecular hydrogels.

Clay-based functional hydrogels were facilely prepared via a bioinspired approach. Montmorillonite (clay) was exfoliated into single layers in water and then coated with a thin layer of polydopamine (PDOPA) via in situ polymerization of dopamine under basic aqueous conditions. When a small amount of ferric salt was added into aqueous suspensions of the polydopamine-coated clay (D-clay), D-clay and Fe(3+) ions could rapidly self-assemble into three-dimensional networks through the formation of coordination bonds. Consequently, supramolecular hydrogels were formed at very low D-clay contents. Rheological measurements show that the D-clay/Fe(3+) hydrogels exhibit fairly elastic response in low stain range, and have self-healing capability upon removal of applied large stress. More importantly, the hydrogels can be used as adsorbents to effectively remove Rhodamine 6G (Rh6G), an organic pollutant, from water. UV-vis absorption spectra of the Rh6G-loaded hydrogels show bands related to π-π stacking interactions between the aromatic moieties of PDOPA and Rh6G, confirming the formation of PDOPA/Rh6G complex on the surface of D-clay.

A Comparison Study on Toughening Vinyl Ester Resins Using Different Nanocarbon Materials.

This study aims to comprehensively compare and evaluate the toughening effects of different nanocarbon materials on vinyl ester resins. Four typical nanocarbon materials, including graphene, graphene oxide (GO), single-walled carbon nanotubes (SWCNTs), and multi-walled carbon nanotubes (MWCNTs), were used as reinforcing fillers for vinyl ester resins. These four nanocarbon materials were dispersed in the vinyl ester resin matrix by the combination of high-speed stirring and probe sonication, and their dispersion states were observed with optical microscopy. The effects of incorporating different nanocarbon materials on the viscosities, thermal properties, tensile properties, and fracture toughness of the resulting modified vinyl ester resins were systematically investigated. The results indicate that the four nanocarbon materials show enhanced toughening effects on the vinyl ester resin in the sequence of SWCNTs, GO, MWCNTs, and graphene. Compared with the control resin, the modified vinyl ester resin containing 0.2 wt% graphene shows 45% and 54% enhancements in the critical stress intensity factor (KIC) and critical strain energy release rate (GIC), respectively. The incorporation of the four nanocarbon materials has almost no effect on the glass transition temperatures of the resulting modified vinyl ester resins. This study provides valuable insights into the selection of nanocarbon additives for enhancing the toughness of vinyl ester resins.

Hemiaminal dynamic covalent networks with rapid stress relaxation, reprocessability and degradability endowed by the synergy of disulfide and hemiaminal bonds.

This work proposes a strategy to address the challenge of achieving rapid reprocessability of vitrimers at mild temperatures by introducing dynamic disulfide and hemiaminal bonds into hemiaminal dynamic covalent networks (HDCNs). The resulting HDCNs, termed HDCNs-DTDA, were prepared through a facile polycondensation between formaldehyde and 4,4'-dithiodianiline. The dual dynamic bond system in the HDCNs-DTDA enables rapid stress relaxation under mild temperature (65 °C for 54 s), which is significantly faster than that observed in HDCNs containing a single dynamic bond (HDCNs-DDM). The HDCNs-DTDA also exhibit a glass transition temperature of 96 °C, excellent solvent resistance and high recovery rates (97%) of tensile strength after reprocessing. In addition, HDCNs-DTDA can be easily degraded in HCl and thiol solutions at room temperature to enable chemical recyclability. Finally, HDCNs-DTDA demonstrates fast shape memory behaviors using thermal stimulation.

Severe fever with thrombocytopenia syndrome incidence could be associated with ecotone between forest and cultivated land in rural settings of central China.

Severe fever with thrombocytopenia syndrome (SFTS), an emerging tick-borne disease first reported in rural areas of central China, has become a major public health concern in endemic areas. The epidemic dynamic and ecologic factors of SFTS incidence at a village scale remain unclear. Here we analyzed the epidemiological characteristics of SFTS cases in Shangcheng County, the first reported areas of SFTS in China. A retrospective space-time cluster analysis was conducted to identify the dynamics of hotspot areas, and the negative binomial regression model was conducted to examine potential factors contributing to the incidence of SFTS at the village level. A total of 1,219 SFTS cases were reported in Shangcheng County from 2011 to 2020, with a case fatality rate of 12.0%. The median age of patients was 64 years, and 81.7% of patients were over 50 years old. Women accounted for 60.3% of all cases, and the incidence rate was significantly higher than that of men (Pearson χ2 test, P<0.001). Five spatial-temporal clusters were identified, and mostly distributed in the central part of the county. Higher risk of SFTS incidence was shown in villages with higher percentage coverages of forest and tea plantation, and higher goat density. In villages where the ratio of cultivated land area to forest land area was between 0.2 and 1.2, the risk of SFTS incidence increased significantly, with an incidence rate ratio of 1.33 (95% CI: 1.04‒1.72, p = 0.024). Our findings indicated that ecotone between forest and cultivated land might be the most important risk settings for exposure and infection with SFTS virus in endemic areas of central China. Precise identification of risk factors and high-risk areas at a suitable scale is conducive to carrying out targeted measures and improving the surveillance of the disease.

A sustainable and low pollutive strategy for the recycling of waste hot-gas filter bags: The development of filter reinforced epoxy composites.

The fast accumulation of waste hot-gas filter bags has become a growing public concern considering its difficulty in degradation, severe pollution elicited by landfill and incineration, high energy consumption during burning or complicated recycling and low margin of regenerative products. Herein, we provide a new feasible recycling strategy by directly employing the cleaned polyphenylene sulfide (PPS) /polytetrafluoroethylene (PTFE) waste filters in their fabric state as the reinforcement of epoxy composites. Merely two layers of filters could produce composites with flexural strength and modulus sufficient for many applications and the additional carbon fiber fabric (CFF) covering could further strengthen the composites (295 to 1010 % increments). The filters also showed a bonding promotion function between CFF and polymethacrylimide foam in lightweight composites. After hydrothermal treatment, the composites reinforced by the recycled filters displayed 97.2 % and 90.9 % retention rate for flexural strength and modulus, respectively. Compared to the pure epoxy, the composites could achieve a limiting oxygen index of 27.6 %, and display 24 % decline in thermal energy release and 20.0 to 31.0 % reduction in the generation rate of combustion products, indicating strengthened flame-retardancy. With shortened processes and elevated properties of composites, the approach established for recycling waste filters in this work showed far-reaching implications in carbon emission reduction, environmental pollution diminishing and commercialization potential.

Highly Elastic and Strain Sensing Corn Protein Electrospun Fibers for Monitoring of Wound Healing.

Due to the lack of sufficient elasticity and strain sensing capability, protein-based ultrafine fibrous tissue engineering scaffolds, though favorable for skin repair, can hardly fulfill on-spot wound monitoring during healing. Herein, we designed highly elastic corn protein ultrafine fibrous smart scaffolds with a three-layer structure for motion tracking at an unpackaged state. The densely cross-linked protein networks were efficiently established by introducing a highly reactive epoxy and provided the fiber substrates with wide-range stretchability (360% stretching range) and ultrahigh elasticity (99.91% recovery rate) at a wet state. With the assistance of the polydopamine bonding layer, a silver conductive sensing layer was built on the protein fibers and endowed the scaffolds with wide strain sensing range (264%), high sensitivity (gauge factor up to 210.55), short response time (<70 ms), reliable cycling stability, and long-lasting duration (up to 30 days). The unpackaged smart scaffolds could not only support cell growth and accelerate wound closure but also track motions on skin and in vivo and trigger alarms once excessive wound deformations occurred. These features not only confirmed the great potential of these smart scaffolds for applications in tissue reconstruction and wound monitoring but also proved the possibility of employing various plant protein ultrafine fibers as flexible bioelectronics.

Water insoluble and flexible transparent film based on carboxymethyl cellulose.

Preparation of renewable, insoluble, and transparent films is still a major challenge for the application of soft electronics and packing industry. Herein, a "green" protocol for preparation of such a film based on carboxymethyl cellulose (CMC) is presented, where acid assistant freeze-thaw method was used in combination with drying. We have shown that the resultant films displayed flexibility, high light transmittance (above 90 %), insolubility, high mechanical performances (elastic modulus of 29.6 MPa), and good thermal stability. Moreover, CMC film/filter paper was fabricated, and the waterproof and mechanical properties of which were investigated. This approach offers a promising route to the fabrication of flexible and transparent films with good waterproof properties based on soluble biomass.

A Comprehensive Study on the Mechanical Properties of Different 3D Woven Carbon Fiber-Epoxy Composites.

In this work, the tensile, compressive, and flexural properties of three types of 3D woven composites were studied in three directions. To make an accurate comparison, three 3D woven composites are made to have the same fiber volume content by controlling the weaving parameters of 3D fabric. The results show that the 3D orthogonal woven composite (3DOWC) has better overall mechanical properties than those of the 3D shallow straight-joint woven composite (3DSSWC) and 3D shallow bend-joint woven composite (3DSBWC) in the warp direction, including tension, compression, and flexural strength. Interestingly their mechanical properties in the weft direction are about the same. In the through-thickness direction, however, the tensile and flexural strength of 3DOWC is about the same as 3DSBW, both higher than that of 3DSSWC. The compressive strength, on the other hand, is mainly dependent on the number of weft yarns in the through-thickness direction.

Reprocessable, Reworkable, and Mechanochromic Polyhexahydrotriazine Thermoset with Multiple Stimulus Responsiveness.

Developing recyclable, reworkable, and intelligent thermosetting polymers, as a long-standing challenge, is highly desirable for modern manufacturing industries. Herein, we report a polyhexahydrotriazine thermoset (PHT) prepared by a one-pot polycondensation between 4-aminophenyl disulfide and paraformaldehyde. The PHT has a glass transition temperature of 135 °C and good solvent resistance. The incorporation of dual stimuli-responsive groups (disulfide bond and hexahydrotriazine ring) endows the PHT with re-processability, re-workability, and damage monitoring function. The PHT can be repeatedly reprocessed by hot pressing, and a near 100% recovery of flexural strength is achieved. The PHT can also degrade in inorganic acid or organic thiol solutions at room temperature. The thermally reworkable test demonstrates that, after heating the PHT at 200 °C for 1 h, the residuals can be easily wiped off. Finally, the PHT exhibits a reversible mechanochromic behavior when damaged.

Three-dimensional rope-like and cloud-like nanofibrous scaffolds facilitating in-depth cell infiltration developed using a highly conductive electrospinning system.

Three-dimensional (3D) nanofibrous scaffolds are at the forefront of tissue engineering research. However, owing to the compact geometries or unstable reserved pores, the scaffolds produced by the current techniques provide limited in-depth cell infiltration, leaving the regeneration of 3D tissues a major challenge. Herein, we have developed a novel single-step 3D electrospinning technique to create 3D rope-like or cloud-like nanofibrous scaffolds by introducing 0 to 0.9 wt% of silver nanoparticles (Ag NPs) into a spinning system and provided an insight into the mechanism. The incorporation of Ag NPs caused intense jet whipping and elevated fiber conductivity, allowing reverse charge transfer and segmented charge storage to provoke vertical collection of waved spirals. The resultant scaffolds exhibited ultrahigh specific pore volumes, facilitating in-depth cell attachment, migration, and proliferation. This work demonstrated a feasible approach to establish versatile 3D culture nanofibrous platforms for a variety of biomedical applications.

Sustained Local Delivery of Diclofenac from Three-Dimensional Ultrafine Fibrous Protein Scaffolds with Ultrahigh Drug Loading Capacity.

The three-dimensional (3D) ultrafine fibrous scaffolds loaded with functional components can not only provide support to 3D tissue repair, but also deliver the components in-situ with small dosage and low fusion frequency. However, the conventional loading methods possess drawbacks such as low loading capacity or high burst release. In this research, an ultralow concentration phase separation (ULCPS) technique was developed to form 3D ultrafine gelatin fibers and, meanwhile, load an anti-inflammatory drug, diclofenac, with high capacities for the long-term delivery. The developed scaffolds could achieve a maximum drug loading capacity of 12 wt.% and a highest drug loading efficiency of 84% while maintaining their 3D ultrafine fibrous structure with high specific pore volumes from 227.9 to 237.19 cm3/mg. The initial release at the first hour could be reduced from 34.7% to 42.2%, and a sustained linear release profile was observed with a rate of about 1% per day in the following 30 days. The diclofenac loaded in and released from the ULCPS scaffolds could keep its therapeutic molecular structure. The cell viability has not been affected by the release of drug when the loading was less than 12 wt.%. The results proved the possibility to develop various 3D ultrafine fibrous scaffolds, which can supply functional components in-situ with a long-term.

A One-Component, Fast-Cure, and Economical Epoxy Resin System Suitable for Liquid Molding of Automotive Composite Parts.

Imidazole cured epoxy resin systems were evaluated for one-component, fast-curing resins for liquid molding of automotive composite parts according to industry requirements. It was demonstrated that an epoxy resin-1-(cyanoethyl)-2-ethyl-4-methylimidazol(EP-1C2E4MIM) system would cure in a few minutes at 120 °C, while exhibiting acceptable pot life, viscosity profiles, and low water absorption. Moreover, this system yielded high Tg parts with mechanical properties similar to the amine-epoxy systems, which are the mainstream two-component epoxy resin systems for automobiles.

Sulfonic Acid- and Lithium Sulfonate-Grafted Poly(Vinylidene Fluoride) Electrospun Mats As Ionic Liquid Host for Electrochromic Device and Lithium-Ion Battery.

Electrospun polymer nanofibrous mats loaded with ionic liquids (ILs) are promising nonvolatile electrolytes with high ionic conductivity. The large cations of ILs are, however, difficult to diffuse into solid electrodes, making them unappealing for application in some electrochemical devices. To address this issue, a new strategy is used to introduce proton conduction into an IL-based electrolyte. Poly(vinylidene fluoride-co-hexafluoropropylene) (P(VDF-HFP)) copolymer is functionalized with sulfonic acid through covalent attachment of taurine. The sulfonic acid-grafted P(VDF-HFP) electrospun mats consist of interconnected nanofibers, leading to remarkable improvement in dimensional stability of the mats. IL-based polymer electrolytes are prepared by immersing the modified mats in 1-butyl-3-methylimidazolium tetrafluoroborate (BMIM(+)BF4(-)). It is found that the SO3(-) groups can have Lewis acid-base interactions with the cations (BMIM(+)) of IL to promote the dissociation of ILs, and provide additional proton conduction, resulting in significantly improved ionic conductivity. Using this novel electrolyte, polyaniline-based electrochromic devices show higher transmittance contrast and faster switching behavior. Furthermore, the sulfonic acid-grafted P(VDF-HFP) electrospun mats can also be lithiated, giving additional lithium ion conduction for the IL-based electrolyte, with which Li/LiCoO2 batteries display enhanced C-rate performance.

Fe/N/C hollow nanospheres by Fe(iii)-dopamine complexation-assisted one-pot doping as nonprecious-metal electrocatalysts for oxygen reduction.

In this work, a series of hollow carbon nanospheres simultaneously doped with N and Fe-containing species are prepared by Fe(3+)-mediated polymerization of dopamine on SiO2 nanospheres, carbonization and subsequent KOH etching of the SiO2 template. The electrochemical properties of the hollow nanospheres as nonprecious-metal electrocatalysts for oxygen reduction reaction (ORR) are characterized. The results show that the hollow nanospheres with mesoporous N-doped carbon shells of ∼10 nm thickness and well-dispersed Fe3O4 nanoparticles prepared by annealing at 750 °C (Fe/N/C HNSs-750) exhibit remarkable ORR catalytic activity comparable to that of a commercial 20 wt% Pt/C catalyst, and high selectivity towards 4-electron reduction of O2 to H2O. Moreover, it displays better electrochemical durability and tolerance to methanol crossover effect in an alkaline medium than the Pt/C. The excellent catalytic performance of Fe/N/C HNSs-750 towards ORR can be ascribed to their high specific surface area, mesoporous morphology, homogeneous distribution of abundant active sites, high pyridinic nitrogen content, graphitic nitrogen and graphitic carbon, as well as the synergistic effect of nitrogen and iron species for catalyzing ORR.

Lignin-assisted exfoliation of molybdenum disulfide in aqueous media and its application in lithium ion batteries.

In this article, alkali lignin (AL)-assisted direct exfoliation of MoS2 mineral into single-layer and few-layer nanosheets in water is reported for the first time. Under optimized conditions, the concentration of MoS2 nanosheets in the obtained dispersion can be as high as 1.75 ± 0.08 mg mL(-1), which is much higher than the typical reported concentrations (<1.0 mg mL(-1)) using synthetic polymers or compounds as surfactants. The stabilizing mechanism primarily lies in the electrostatic repulsion between negative charged AL, as suggested by zeta-potential measurements. When the exfoliated MoS2 nanosheets are applied as electrode materials for lithium ion batteries, they show much improved electrochemical performance compared with the pristine MoS2 mineral because of the enhanced ion and electron transfer kinetics. This facile, scalable and eco-friendly aqueous-based process in combination with renewable and ultra-low-cost lignin opens up possibilities for large-scale fabrication of MoS2-based nanocomposites and devices. Moreover, herein we demonstrate that AL is also an excellent surfactant for exfoliation of many other types of layered materials, including graphene, tungsten disulfide and boron nitride, in water, providing rich opportunities for a wider range of applications.

From waste to functional additive: toughening epoxy resin with lignin.

A novel approach to toughen epoxy resin with lignin, a common waste material from the pulp and paper industry, is presented in this article. First, carboxylic acid-functionalized alkali lignin (AL-COOH) was prepared and subsequently incorporated into anhydride-cured epoxy networks via a one-pot method. The results of mechanical tests show that covalent incorporation of rigid AL-COOH into epoxy networks can significantly toughen the epoxy matrix without deteriorating its tensile strength and modulus. The addition of 1.0 wt % AL-COOH gives increases of 68 and 164% in the critical stress intensity factor (K(IC)) and critical strain energy release rate (G(IC)), respectively, relative to that of neat epoxy. This article opens up the possibility of utilizing low-cost and renewable lignin feedstocks as effective toughening agents for thermoset polymers.

Highly conductive graphene by low-temperature thermal reduction and in situ preparation of conductive polymer nanocomposites.

Polydopamine-coated graphene oxide (DGO) films exhibit electrical conductivities of 11,000 S m(-1) and 30,000 S m(-1) upon vacuum annealing at 130 °C and 180 °C, respectively. Conductive poly(vinyl alcohol)/graphene and epoxy/graphene nanocomposites show low percolation thresholds due to the excellent dispersibility of the DGO sheets and their effective in situ reduction.

Microporous polyimide networks with large surface areas and their hydrogen storage properties.

Microporous polyimide networks with BET surface areas up to 1407 m(2) g(-1) and pore size distribution of 4-8 Å were synthesized. The respective effect of surface area and affinity between hydrogen molecule and polyimides on hydrogen storage properties were investigated.