Clostridium beihaiense sp. nov., an anaerobic bacterium isolated from activated sludge.

A Gram-positive, strictly anaerobic, rod-shaped bacterium, designated YB-7T, was isolated from activated sludge of an anaerobic baffled reactor pond in Weizhou terminal wastewater treatment plant, Beihai, Guangxi, China. Strain YB-7T grew at pH 5.0-12.0 (optimum, pH 7.0), 20-45 °C (37 °C) and NaCl concentration of 0-5 % w/v (optimum, 5 %). 16S rRNA gene sequence analysis results showed that strain YB-7T belonged to the genus Clostridium and it was most closely related to Clostridium tetanomorphum DSM 4474T (96.9 % similarity). The DNA-DNA relatedness of strain YB-7T to Clostridium tetanomorphum DSM 4474T was 47.4 %. The DNA G+C content of strain YB-7T was determined to be 32.3 mol%, and the predominant cellar fatty acid (>10 %) was C16 : 0. Polar lipids of strain YB-7T included diphosphatidylglycerol, phosphatidylethylethanolamine, phosphatidylethanolamine, phosphatidylglycerol, phosphatidylcholine, two unidentified aminophospholipids, two unidentified phospholipids and unidentified lipids. The results of this study supported the conclusion that strain YB-7T should be assigned to a new member of the genus Clostridium, for which the name Clostridium beihaiense sp. nov. is proposed. The type strain is YB-7T (=CICC 24109T=KCTC 15555T).

Distribution characteristics of organic carbon (nitrogen) content, cation exchange capacity, and specific surface area in different soil particle sizes.

Understanding the distribution of soil organic carbon and nitrogen (OC(N)) content, cation exchange capacity (CEC), and specific surface area (SSA) in different soil particle sizes is crucial for studying soil fertility and properties. In this study, we investigated the distribution characteristics of the OC(N), CECand SSA in different particles of yellow-brown soil under different methods. The result revealed that as the particle size decreased, the soil OC(N), SSA and CEC content gradually increase. The content of OC and ON different soil particles ranged from 1.50-28.16 g·kg-1 to 0.18-3.78 g·kg-1, respectively, and exhibited significant differences between different particles. We observed good linear relationships between OC and ON in different particle sizes of yellow-brown soil under different utilization methods, with correlation coefficients ranging from 0.86 to 0.98, reaching a very significant level (n = 12, p < 0.01). The ranges of SSA and CEC in different particles of the four soils were 0.30-94.70 m2·g-1 and 0.70-62.91 cmol·kg-1, respectively. Additionally, we found logarithmic relationships between SSA (CEC) and the equivalent diameter for the four soils, with correlation coefficients (r2) higher than 0.91. Furthermore, there was an extremely significant linear relationship between CEC and SSA of the four soils, with correlation coefficients (r2) of 0.92-0.97 (n = 12, p < 0.01). These results highlight the close relationship between soil particle size and soil OC(N), SSA, and CEC. The conclusions drawn from this study provide valuable data support and a theoretical basis for further understanding soil properties.

Two-step hydrothermal synthesis and conversion mechanism of zeolite X from stellerite zeolite.

We investigated the conversion mechanism of stellerite zeolite to zeolite X under two-step hydrothermal conditions. To elucidate the conversion mechanism, solid products were separated from the mixtures at different crystallization times and characterized by XRD, FESEM, FT-IR, Raman, solid-state NMR, XRF, and TEM. The results indicate that in this reaction process, the Si, Al, and Na in the gel solid phases were continuously dissolved and transformed into the gel-liquid-phase. When the concentration of each component reached supersaturation in the gel-liquid-phase, Si, Al, and Na were transferred to the surface of the gel-solid-phase, and nucleation and crystallization occurred on the surface. Abundant nuclei were formed during the second hour of the crystallization. As the crystallization time increased, the nuclei rapidly grew into zeolite X crystals, and the relative crystallinity of zeolite X reached a maximum when the crystallization time reached 4 h. These phenomena indicate that the formation mechanism of zeolite X is a liquid-phase conversion mechanism.

Efficient methane production from waste activated sludge and Fenton-like pretreated rice straw in an integrated bio-electrochemical system.

Integrated microbial electrolysis cell-anaerobic digestion (MEC-AD) systems have demonstrated potential advantages for methane production in the presence of small amounts of residual inhibitors. In this study, a series of tests were conducted to analyse the acidification and methanogenesis performance of pretreated rice straw (RS) in anaerobic digestion (AD) and MEC-AD systems after the addition of Fenton-like reagents. The results indicated that the short-chain acids (SCFAs) accumulations reached 2284.64 ± 21.57 mg COD/L with a dosage ratio of 1/4 (g RS/g VSS sludge) in the MEC-AD system and that methane production increased by 63.8% compared with that of an individual AD system. In the interim, the net energy output reached 1.09 × 103 J/g TCOD, which was 1.23 times higher than that of the AD system. The residual Fe3+/Fe2+ in the pretreatment reagent was capable of promoting acidification and methanogenesis in sludge and RS fermentation. The RS hydrolysis products could constrain methanogenesis, which can be mitigated by introducing an MEC. The microbiological analyses revealed that the MEC strongly increased the enrichment of hydrogenotrophic methanogens, especially Methanobacterium (61.16%). Meanwhile, the Syntrophomonas and Acetobacterium abundances increased to 2.81% and 2.65%, respectively, which suggested the reinforcement of acetogenesis and methanogenesis. Therefore, the enhanced hydrogenotrophic methanogens might have served as the key for enhancing the efficiency of methanogenesis due to the introduction of an MEC.

Adsorption of As(V) from Aqueous Solution on Chitosan-Modified Diatomite.

A novel chitosan (CS)-modified diatomite (Dt) was prepared by a simple mixture in the mass ratio to remove As(Ⅴ) from aqueous solution in this research. The CS-modified Dt adsorbent was characterized by scanning electron microscopy (SEM), Fourier-transform infrared spectroscopy (FTIR), and X-ray powder diffraction (XRD) analysis. The parameters to influence the adsorption of As(Ⅴ) ion were studied under such conditions as kinetics, adsorption isotherm, and pH effect. The results revealed that adsorption of As(Ⅴ) was initially rapid and the equilibrium time was reached after 40 min. The optimal value of the pH was 5.0 for better adsorption. The equilibrium data were well fitted to the Langmuir isotherm compared to the Freundlich isotherm, and exhibited the highest capacity and removal efficiency of 94.3% under an initial As(Ⅴ) concentration of 5 mg/L. The kinetic data were well described by the pseudo-second-order model. In addition, 0.1 M NaOH has the best desorption efficiency of As(V) adsorbed on CS-modified Dt, and the removal efficiency of As(V) was still higher than 90% when after six adsorption-desorption cycles. These results showed that the CS-modified Dt could be considered as a potential adsorbent for the removal of As(V) in aqueous solution.