To apply hydrotalcites more effectively to the problem of dye wastewater, the effects of divalent metal ions on the structure and stability of hydrotalcites, especially on their photocatalytic activity, were compared. In the present study, M/Cr hydrotalcites (M3Cr-CO3-LDHs) (in which M = Mg, Co, Ni, Cu, Zn), where the M/Cr molar ratio was 3, were prepared by the co-precipitation method. The structures and properties were characterized using powder X-ray diffraction (XRD), Fourier-transform infrared spectroscopy (FTIR), thermogravimetric-differential thermal analysis (TG-DTA), and UV-Visible diffuse reflectance spectroscopy (UV-Vis DRS). The results showed that five kinds of M3Cr-CO3-LDHs were synthesized successfully, and the layered structure of the samples obtained was regular and the crystal phase was single. When methylene blue (MB) solution was exposed to ZnCr-CO3-LDHs, H2O2, and visible light irradiation, more than 90.67% of the methylene blue (MB) was removed after 140 min. The photocatalytic activity of the samples was in the order: Co3Cr-CO3-LDHs > Mg3Cr-CO3-LDHs > Cu3Cr-CO3-LDHs > Zn3Cr-CO3-LDHs > Ni3Cr-CO3-LDHs. The results of a catalytic mechanism study showed that photocatalytic degradation of MB involved a demethylation reaction, with the reactive species containing •O2-, •OH, and h+.

The reform era began with the removal of Mao-era elites from leadership positions on a scale theretofore unseen in the People's Republic of China. Rather than depending on incentives to mobilize Mao-era cadres to support Reform and Opening, the new reform leadership brought in younger, better educated pro-reform elites. This article thus proposes a Personnel Model, in which the Communist Party brings in sympathetic cadres to implement major shifts in the Party line. Furthermore, personnel changes were first imposed on the military, then on the civilian apparatus. We show the large scale and rapid implementation of these reforms in 1982–1984 using an original database of over 60,000 cadres drawn from Organizational Histories.

Bullfrog is one of the most important economic aquatic animals in China that is widely cultured in southern China and is a key breed recommended as an industry of poverty alleviation in China. During recent years, a fatal bacterial disease has often been found in cultured bullfrogs. The clinical manifestations of the diseased bullfrogs were severe intestinal inflammation and an anal prolapse. A bacterial pathogen was isolated from the diseased bullfrog intestines. The bacterium was identified as Vibrio cholerae using morphological, biochemical and 16S rRNA phylogenetic analysis. In this study, V. cholerae was isolated and identified in diseased bullfrogs for the first time, providing a basis for the diagnosis and control of the disease. Therefore, attention should be paid to the modes of transmission of V. cholerae from bullfrog and formulate reasonable safety measures.

Graphene-based flexible and wearable supercapacitors have been produced by wet spinning, in which organic solvent coagulating bath was prerequisite and spacers were usually incorporated to improve the electrochemical property but sacrificing the mechanical property. In this work, a nonorganic solvent spinning technology named as interfacial polyelectrolyte complexation (IPC), which was based on the spontaneous self-assembly of two oppositely charged polyelectrolyte solutions/suspensions to form continuous fibers on drawing in their interfaces, was proposed to fabricate graphene fiber–shaped electrodes for supercapacitors. Due to the excellent mechanical performance and hydrophilicity, cellulose nanofibrils (CNFs) were added to serve as an efficient reinforcing agent and spacer of graphene fiber electrodes. Consequently, the mechanical performance and specific capacitance of the fibers were improved but electrical conductivity was declined. Taking overall consideration, CNF/rGO60 fiber electrode possessed a superior integrated performance with a capacitance of 182.6 F/g, tensile strength of 480 MPa, and electrical conductivity of 5538.7 S/m. The IPC spinning provided an environmentally friendly strategy for the fabrication of fiber-shaped functional devices.

The purpose of this study was to develop a simple and economic method for the preparation of porous bioceramics with controllable macrostructure. Raw materials, including very small organic foam balls as the pore-creating reagent, wax (or paraffin) as the solvent, and oleic acid as the surface active agent, were selected along with bioactive materials such as β-TCP ceramic powder as the main component. The selected components were mixed into a slurry at 30–120ºC and shaped into a green body with a hot die-casting machine at 30–90ºC. The green body was then sintered and porous bioceramics were obtained. The main characteristics of porous bioceramics such as weight loss, compressive strength, connection and size of pores, percolation rate of water, apparent porosity and bulk density were measured. The results indicated that the apparent porosity and the specific surface area were large; the pores were connected in three dimensions and the compressive strength was >1.6 MPa. This study demonstrated that the methods used here are simple and effective in generating porous bioceramics with controllable macrostructures.

This study focuses on the main factors determining the apparent porosity of porous bioceramics prepared using small organic foam spheres as the pore-making reagent, in order to determine the best technical parameters for preparing porous bioceramics. In every experiment, only one of these factors (the time of heating, the sintering temperature, the mass ratio between small organic foam spheres and beta-tricalcium phosphate (β-TCP) powder, and the rate of the temperature rise) was changed, while the others were kept constant. In each case the apparent porosity was tested and the relation between the specific variable and apparent porosity was observed. Finally, the optimum technical parameters were deduced. The apparent porosity shows an inverse linear relation to the time of heating and the sintering temperature, and is approximately proportional to the mass ratio between the small organic foam spheres and the β-TCP powder and the rate of temperature rise. These factors have important influences on the apparent porosity. The optimum conditions were: heating time (soak time) 120 min, sintering temperature 850ºC, mass ratio 0.25, and a rate of temperature increase of 120ºC h–1.

The purpose of this study was to develop a simple and efficient method for manufacturing porous bioceramics, in which small organic foam spheres were taken as the poremaking reagent and green bodies were made by hot die-casting in moulds. The raw materials (small organic foam spheres, paraffin, oleic acid and β-TCP powder) were mixed into a slurry at 30–120ºC and moulded into green bodies using a hot die-casting machine at 30–90ºC; the green bodies were then sintered and the porous bioceramics obtained. The main characteristics (structure and size of pores, water permeability, apparent porosity and shrinkage) were tested. The results indicated that the apparent porosity was high and directly proportional to the mass ratio between the small organic foam spheres and the β-TCP powder. The pores connected with each other in three dimensions; the size, distribution of the shapes and structures of the pores were clearly related to the dimensions of the small organic foam spheres. The water permeability was proportional to the hot die-casting pressures and the shapes of the samples could easily be controlled by selecting different moulds. This study indicated that the method can be used to manufacture porous bioceramics with controlled pore structures and different shapes effectively and easily by adding different amounts and sizes of small organic foam spheres, mixing the raw materials evenly, and by selection of the hot die-casting pressure and by the use of different moulds.

The development of highly efficient and stable inexpensive catalysts for the reduction of 4-nitrophenol (4-NP) to 4-aminophenol (4-AP) by NaBH4 in an aqueous solution by utilizing metal-organic frameworks (MOFs) as precursor and template remains a hot topic. Herein, a simple self-template strategy was developed to synthesize a porous nitrogen-doped carbon frameworks embedded with zinc and cobalt nanoparticles (Zn0.3Co2.7@NC) catalyst by thermal annealing of the bimetallic zinc-cobalt zeolitic imidazolate framework (Zn0.3Co2.7-ZIF) as an effective precursor and template. The resulting Zn0.3Co2.7@NC catalysts show an excellent catalytic activity for the reduction of 4-NP and the reduction reaction was completed only in 5 min with nearly 100% conversion. The apparent rate constant for the reaction of 4-NP reduction was estimated to be 0.683 min−1. Moreover, the catalyst was extended to reduce other nitro compounds and exhibited excellent catalytic activity. When compared to other related catalysts in the literature, the catalytic activity of catalyst is superior. Therefore, the resulting Zn0.3Co2.7@NC is expected to get more extensive application in the field of catalysis.

During its structural transformation, rural China witnessed the emergence of four types of village: traditional, industrialized, commercial and villages in cities. Information Communication Technologies (ICTs), including fixed phones, cell phones, television sets and the internet (with personal computers), are now commonly used in Chinese villages but in ways that differentiate villagers according to variables such as occupation, villager membership and social status. The adoption of ICTs by peasants not only represents but also accelerates growing peasant differentiation; in other words, the function of ICTs could not penetrate the barrier of social structure. Meanwhile, structural transformation in China has been an activator to shaping peasants' diversified ideas about information, and the demand for and usage of ICTs. An analysis of peasants' ICT adoption thus enables us to identify the basic trends and characteristics of social transformation in contemporary China.

The (ZnSe) /(ZnS ), strained layer super-lattices (SLSs) on (100) GaAs and (ZnTe)/(ZnSe) SLSs on (100) InP have been grown by molecular beam epitaxy (MBE) and atomic layer epitaxy (ALE). The structural characteristics of these SLSs were investigated in situ RHEED observation, low-angle X-ray diffraction spectra, TED image and AES analysis. The optical properties of the SLSs, such as refractive index of superlattice materials, photoluminescence (PL) spectra, transient PL spectra, Raman spectra, far-infrared reflectivity spectra and Optical nonlinear have been studied.