Inducing Circularly Polarized Luminescence by Confined Synthesis of Ultrasmall Chiral Carbon Nanodot Arrays in Pyrene-Based MOF Thin Film.

Combining the features of the host-guest system and chirality is an efficient strategy to achieve circularly polarized luminescence (CPL). Herein, well-defined chiral carbon nanodot (chirCND) arrays were confined-synthesized by low-temperature calcination of a chiral amino acid loaded metal-organic framework (MOF) to induce high CPL. An achiral porous pyrene-based MOF NU-1000 thin film as the host template was prepared by a liquid-phase epitaxial layer-by-layer fashion, and chiral amino acids as the carbon sources could be confined in the porous MOF and carbonized to homogeneous and ultrasmall chirCND arrays, resulting in a chirCNDs@NU-1000 thin film (l-CNDsx@NU-1000; x = l-cysteine (cys), l-serine, l-histidine, l-glutamic acid, and l-pyroglutamic acid). The results show the pristine chirCNDs by directly carbonizing chiral amino acids hardly endow them with a CPL property. By contrast, benefiting from the arrayed confinement and coordination interaction between chirCNDs and NU-1000, the chirality transfer on the excited state of chirCNDs@NU-1000 is enabled, leading to strong CPL performance (a high luminescence dissymmetry factor glum of l-CNDscys@NU-1000 thin film reached 1.74 × 10-2). This study of chirCNDs encapsulated in fluorescent MOF thin films provides a strategy for developing uniform chiral carbon nanoarrays and offers chiral host-guest thin-film materials for optical applications.

Boosting Activity and Selectivity of UiO-66 through Acidity/Alkalinity Functionalization in Dimethyl Carbonate Catalysis.

The acid-base properties of supports have an enormous impact on catalytic reactions to regulate the selectivity and activity of supported catalysts. Herein, a train of Pd-X-UiO-66 (X = NO2 , NH2 , and CH3 ) catalysts with different acidity/alkalinity functional groups and encapsulated Pd(II) species is first developed, whose activities in dimethyl carbonate (DMC) catalysis are then investigated in details. Thereinto, the Pd-NO2 -UiO-66 catalyst with acidity functionalization exhibits the best catalytic behavior: the DMC selectivity stemmed from methyl nitrite (MN) is up to 68%, the conversion of CO is 73.4%. The obtained experimental results demonstrate that the NO2 group not only affected the interaction between X-UiO-66 and Pd(II) active sites but also play an indispensable role in the adsorption and activation of MN and CO, which remarkably promote the formation of the COOCH3 * intermediate and DMC product.

Recombinant characteristics, pathogenicity, and viral shedding of a novel PRRSV variant derived from twice inter-lineage recombination.

Porcine reproductive and respiratory syndrome (PRRS), caused by the PRRS virus (PRRSV), is a significant threat to the global pig industry. In this study, a novel recombinant PRRSV, SD043, was isolated from a pig farm experiencing disease in 2019. Phylogenetic analysis revealed that SD043 belonged to lineage 1 of PRRSV-2 while recombination analyses revealed that it is a recombinant virus from lineage 1 and lineage 8 strains. Based on further analysis, SD043 underwent recombination twice. Pathogenicity studies revealed that SD043 causes mild clinical symptoms, thymus atrophy, and severe histopathological lesions in the lungs. Notably, virus shedding in SD043-infected piglets was detectable at 10 days post-inoculation with a high viral load in the respiratory or digestive tract, indicating that the recombinant PRRSV appears to shed higher numbers of virus. Furthermore, genomic surveillance based on all available PRRSVs circulating in Shandong province revealed an increasing increase in recombinant PRRSV since 2015, with the recombinant pattern (between lineages 1 and 8) being the same as that of SD043. These findings enable a better understanding of the process of twice recombination and virus shedding of recombinant PRRSV and can strengthen the prevention and control of the PRRSV epidemic.

Host-Guest Thin Films by Confining Ultrafine Pt/C QDs into Metal-Organic Frameworks for Highly Efficient Hydrogen Evolution.

Combining the features of host templates and guest species is an efficient strategy to optimize the photo/electrocatalytic performance. Herein, novel host-guest thin-film electrocatalysts are designed and developed with Pt doped carbon (Pt/C) confined into porphyrin-based metal-organic frameworks (MOFs). Porous MOF PCN-222 and PCN-221 thin films are used as the host templates and fabricated using vapor-assisted deposition method, and then the guest Pt/C quantum dots are encapsulated into the MOFs by loading the glucose mixed H2 PtCl6 and heating at 200 °C. Thanks to the confinement effect of MOF pores, the homogenous and ultrafine Pt/C nanowires (Pt/CNWs) and nanodots (Pt/CNDs) are confined in nanochannels of PCN-222 and nanocages of PCN-221 (Pt/CNW@PCN-222 and Pt/CND@PCN-221), respectively. The electrocatalytic study shows that the host-guest thin films have highly-efficient electrocatalytic hydrogen evolution performance under light irradiation. Furthermore, the time-resolved photoluminescent results reveal that Pt/CNW@PCN-222 has a faster charge transfer (441 ps) from PCN-222 to Pt/CNWs comparing to that (557 ps) of Pt/CND@PCN-221, indicating the guests with different shapes play an important role in the electrocatalytic performance. This work serves to present both the outstanding level of control in the precise synthesis and high potential for nanocomposite thin films in photo-electrocatalytic application.

Surface-coordinated metal-organic framework thin films (SURMOFs) for electrocatalytic applications.

The design and development of highly efficient electrocatalysts are very important in energy storage and conversion. As a kind of inorganic organic hybrid material, metal-organic frameworks (MOFs) have been used as electrocatalysts in electrocatalytic reactions due to their structural diversities and fascinating functionalities. Particularly, MOF thin films are coordinated on substrate surfaces by a liquid phase epitaxial (LPE) layer by layer (LBL) growth method (called surface-coordinated MOF thin films, SURMOFs), and recently have been studied in various applications due to their precisely controlled thickness, preferred growth orientation and homogeneous surface. In this review, we will summarize the preparation and electrocatalysis of SURMOFs and their derived thin films (SURMOF-D). The SURMOF based thin films possess diverse topological structures and flexible properties, providing abundant catalytically active sites and fast charge transfer for efficient electrocatalytic performance in the oxygen evolution reaction (OER), oxygen reduction reaction (ORR), hydrogen evolution reaction (HER), carbon dioxide reduction reaction (CRR), supercapacitors, tandem electrocatalysis and so on. The research challenges and problems of SURMOFs for electrocatalytic applications are also discussed at the end of the review.

Hydropericardium syndrome outbreak caused by fowl adenovirus serotype 4 in China in 2015.

There have been many outbreaks of hydropericardium syndrome (HPS), which is characterized by pericardial effusion and hepatitis, in Chinese chicken farms since June 2015. HPS was mainly found in miscellaneous meat-type chickens, Ma chickens, layer chicks and Three-yellow chickens, while it was occasionally found in white broilers. To determine the specific causative pathogen and pathogenicity of HPS in chickens, we collected 25 suspected cases and performed clinical pathology and aetiology analyses. The results showed that the 25 cases exhibited multifocal hepatitis with intra-nuclear inclusion bodies and 70 nm-latticed viral particles in the cell nuclei. All samples were positive for fowl adenovirus (FAdV), and sequencing results showed that the hexon gene shared the highest nucleotide similarities with the hexon gene of group 1 serotype 4 (FAdV-4). FAdV-4 was highly pathogenic to embryos and specific pathogen-free chickens, causing 100 and 70 % mortality rates, respectively. Thus, FAdV-4 is associated with HPS outbreaks in China.

Synthesis of La-Co-O Mixed Oxides via Polyethylene Glycol-Assisted Co-Precipitation Method for Total Oxidation of Benzene.

La-Co-O mixed oxides (LCO) were prepared by co-precipitation method with the presence of polyethylene glycol (PEG) as dispersant. The influence of adding different molecular weight of PEG (0, 2 000, 6 000, 20 000 g·mol-1) on the physicochemical and catalytic properties of La-Co-O mixed oxides for total oxidation of benzene was investigated. The samples were characterized by means of N2 physical adsorption, X-ray diffraction (XRD), scanning electron microscopy (SEM), temperature-programmed reduction by H2 (H2-TPR), temperature-programmed desorption of O2 (O2-TPD), and X-ray photoelectron spectroscopy (XPS). The order of catalytic activity was found to be LCO-PEG6000>LCO>LCO-PG20000>LCO-PG2000. Particularly, LCO-PEG6000 exhibited benzene conversion of 99% at temperature as low as 383 ℃, which was 126 ℃ lower than that of LCO. The characterization result reveals that all samples had a BET surface area of about 9～10 m2·g-1. The XRD result shows that on all samples LaCoO3 perovskite was mainly formed together with a small amount of La2O3 and Co3O4. The addition of PEG was favorable for the formation of LaCoO3 perovskite. Particularly, the addition of PEG-6000 effectively suppressed the agglomeration of LaCoO3 perovskite, giving rise to small and uniform particles as observed by SEM. Moreover, the results of H2-TPR and O2-TPD indicate that the obtained La-Co-O mixed oxides showed higher reducibility and lattice oxygen mobility, and the Co 2p XPS analysis suggests that more surface Co3+ active species were presented by the addition of PEG-6000. These properties are thought to contribute to the high activity in benzene total oxidation.

Characterization of antigenic domains and epitopes in the ORF3 protein of a Chinese isolate of avian hepatitis E virus.

Avian hepatitis E virus (HEV) is an emerging virus associated with the big liver and spleen disease or hepatitis-splenomegaly syndrome in chickens and subclinical infections by the virus are also common. The complete genome of avian HEV contains three open-reading frames (ORFs) in which ORF2 protein is part of virus particles and thus contains primary epitopes. Antigenic epitopes of avian HEV ORF2 protein have been described but those associated with the ORF3 have not. To analyze the antigenic domains and epitopes in the ORF3 protein of a Chinese isolate of avian HEV (CaHEV), we generated a series of antigens comprised of the complete ORF3 and also five truncated overlapping ORF3 peptides. The antibodies used in this study were mouse antisera and monoclonal antibodies against ORF3, positive chicken sera from Specific Pathogen Free chickens experimentally infected with CaHEV and clinical chicken sera. Using these antigens and antibodies, we identified three antigenic domains at amino acids (aa) 1-28, 55-74 and 75-88 in which aa 75-88 was a dominant domain. The dominant domain contained at least two major epitopes since field chickens infected with avian HEV produced antibodies against the domain and epitopes. These results provide useful information for future development of immunoassays for the diagnosis of avian HEV infection.

Submerged macrophytes modify bacterial community composition in sediments in a large, shallow, freshwater lake.

Submerged aquatic macrophytes are an important part of the lacustrine ecosystem. In this study, the bacterial community compositions in the rhizosphere sediments from three kinds of submerged macrophytes (Ceratophyllum demersum, Potamogeton crispus, and Vallisneria natans) were investigated to determine whether submerged macrophytes could drive the variation of bacterial community in the eutrophic Taihu Lake, China. Molecular techniques, including terminal restriction fragment length polymorphism (T-RFLP) of PCR-amplified 16S rRNA gene and clone libraries, were employed to analyze the bacterial community compositions. Remarkable differences of the T-RFLP patterns were observed among the different samples, and the results of LIBSHUFF analysis also confirmed that the bacterial community compositions in the rhizosphere sediments of three kinds of submerged macrophytes were statistically different from that of the unvegetated sediment. Acidobacteria, Deltaproteobacteria, and Betaproteobacteria were the dominant bacterial groups in the rhizosphere sediments of Ceratophyllum demersum, Potamogeton crispus, and Vallisneria natans, respectively, accounting for 15.38%, 29.03%, and 18.00% of the total bacterial abundances. Our study demonstrated that submerged macrophytes could influence the bacterial community compositions in their rhizosphere sediments, suggesting that macrophytes have an effect on the cycling and transportation of nutrients in the freshwater lake ecosystem.

[The role of vimentin during PRRSV infection of Marc-145 cells].

The objective of this study was to investigate the function of vimentin in PRRSV infection. Vimentin gene from Marc-145 cells was amplified by RT-PCR, cloned into pET-28a vector and expressed in Escherichia coli BL21(DE3). The expressed vimentin was confirmed by Western blot and purified which was used to immunize BALB/c mice for the production of antibodies. Vimentin and antibodies were tested for blocking PRRSV infection of Marc-145 cells. The binding of vimentin to PRRSV N and GP5 proteins were tested by the ELISA. The results showed that vimentin gene was amplified successfully and expressed as identified by SDS-PAGE and Western blot. Mouse anti-vimentin antibodies were produced with the titer of 10(5). PRRSV infection of Marc-145 cells was blocked partially by vimentin while blocked completely by the antibobies. In addition, vimentin was bound N protein, but not GP5. These results provide additional information on PRRSV entry into Marc-145 cells.

[Determination of palladium in automobile exhaust catalysts by FAAS method].

Palladium in automotive exhaust catalyst was determined by flame atomic absorption spectrometry (FAAS). The analytical conditions and the coexisting elements interference were studied. The catalyst was dissolved by the mixture of H2O2 and HCl. Pd in the solution was directly determined by FAAS method. The linearity of working curve ranges from 0.1 to 15 microg x mL(-1); the detection limit is 0.029 microg x mL(-1); the relative standard deviation (RSD) range is from 0.8% to 2.5%; and the recovery rate range is from 99.6% to 101.2%. It is a simple and convenient method for accurate analysis of Pd in the exhaust catalysts.

[The relationship between structure and oxygen storage capacity of Ce(x)Zr(1-x)O2 solid solution].

Heating reflux aging technology was applied to prepare a series of Ce(x)Zr(1-x)O2 (0.25 < or = x < or = 1) solid solution. The effects of the Ce(x)Zr(1-X)O2 composition on the structure and oxygen storage capacity were characterized using N2 physical adsorp tion, X-ray diffraction (XRD), FT-Raman, UV-Vis diffuse spectroscopy techniques. The texture, structure and thermal stability of ceria-zirconia mixed oxides are closely related to the ratio of cerium to zirconium in the solid solution, with increasing the zirconium content, the specific area increases, and the structure undergoes a change of order --> disorder --> order. Among them, Ce(0.4Zr(0.6)O2 sample possesses the maximum OSC and Ce(0.25)Zr(0.75)O2 sample possesses the best thermal stability.

[Effects of pH value during synthesis on the structure and performance of ceria zirconia mixed oxides].

Heating reflux aging technology was first applied to obtain a series of ceria zirconia mixed oxides composed of 0.6CeO2-0.4ZrO2. N2 physical adsorption, FT-Raman, and UV-Vis diffuse spectroscopy techniques were preformed to investigate the relationships between the structure and oxygen storage capacity of ceria zirconia mixed oxides prepared at different pH value of precipitation. The composition of ceria zirconia mixed oxides fluctuated with the pH value of precipitation, leading to the variation in phase ingredients, defects, crystallization and texture. Controlling the pH value of precipitation at 10.5-11.0 can avoid the introduction of Si, improve the texture, phase homogeneity and defects concentration, decrease the degree of crystallization, and increase the oxygen storage capacity.

[Diffusion reflectance spectroscopy of ZrO2 phase structure].

Diffusion Reflectance Spectroscopy (DRS) was employed to study the surface phase structure of ZrO2-based catalysts. The effect of calcining temperature, and the addition of Al2O3 and platinum on the surface and bulk phase structures of zirconia was studied by DRS combined with XRD, DTA and XPS. The same trend was observed that heating to higher temperatures results in the conversion to monoclinic zirconia in undoped samples, while incorporation of an appropriate amount of Al2O3 would stabilize the tetragonal phase zirconia. And the reduction processing of Pt/ZrO2 affects crystallization and phase transitions, resulting in certain fraction of tetragonal ZrO2 transferred to monoclinic ZrO2. The DRS shows an appreciable difference in the corresponding XRD spectra that more monoclinic zirconia formed on the surface of catalyst during the reduction processing of Pt/ZrO2, compared to the bulk of catalyst.

[Study on the ultraviolet-visible spectra of Au/Al2O3 catalysts].

A variety of synthesis parameters for the preparation of gold nanoparticles by NaBH4 solution reduction in the W/O microemulsion media consisting of Cetyl Trimethyl Ammonium Bromide (CTAB)/n-hexanol/water system was investigated. The results showed that the molar ratio of water to surfactant (rw) had nothing to do with the gold particle size, but the concentration of the aqueous gold salt solution had a significant effect on the size of gold particle. Through optimizing the preparation parameters, Au/Al2O3 catalysts were prepared with two different methods, then the catalysts were characterized by ultraviolet-visible spectra, XRD and TEM, and the effect of two different preparation methods on active component gold particle size in the catalysts was studied.